- Open Access
Intrinsic chemoresistance to gemcitabine is associated with constitutive and laminin-induced phosphorylation of FAK in pancreatic cancer cell lines
© Huanwen et al; licensee BioMed Central Ltd. 2009
- Received: 7 August 2009
- Accepted: 21 December 2009
- Published: 21 December 2009
One of the major reasons for poor prognosis of pancreatic cancer is its high resistance to currently available chemotherapeutic agents. In recent years, focal adhesion kinase (FAK), a central molecule in extracellular matrix (ECM)/integrin-mediated signaling, has been thought to be a key determinant of chemoresistance in cancer cells. In this study, we aimed to determine the roles of FAK phosphorylation in the intrinsic chemoresistance of pancreatic cancer cell lines.
Our results showed that, the level of constitutive phosphorylation of FAK at Tyr397 correlated with the extent of intrinsic resistance to Gemcitabine (Gem) in four pancreatic cancer cell lines. Moreover, in Panc-1 cells, which had high expression of pFAK, specific inhibition of constitutive FAK phosphorylation by either RNAi or FRNK overexpression decreased the phosphorylation of Akt, reduced the levels of survivin expression and Bad phosphorylation at Ser136 and increased Gem-induced cytotoxicity and apoptosis. However, in AsPC-1 cells with a low level of pFAK, neither FAK RNAi nor FRNK overexpression affected Gem-induced cell apoptosis. We further found that laminin (LN) induced FAK and Akt phosphorylation in a time-dependent manner, increased the levels of survivin and pBad (pS136) and decreased Gem-induced cytotoxicity and apoptosis in AsPC-1 cells; Specific inhibition of LN-induced FAK phosphorylation by either FAK RNAi or FRNK overexpression suppressed the effects of LN on AsPC-1 cells. Moreover, inhibition of constitutive FAK phosphorylation in Panc-1 cells and LN-induced FAK phosphorylation in AsPC-1 cells by a novel and more specific FAK phosphorylation inhibitor PF-573,228 showed similar results with those of FAK phosphorylation inhibition by FAK RNAi or FRNK overexpression.
In conclusion, our research demonstrates for the first time that both constitutive and LN-induced FAK phosphorylation contribute to increased intrinsic chemoresistance to Gem in pancreatic cancer cell lines and these effects are partly due to the regulation of Akt and Bad phosphorylation and survivin expression. Development of selective FAK phosphorylation inhibitors may be a promising way to enhance chemosensitivity in pancreatic cancer.
- Focal Adhesion Kinase
- Pancreatic Cancer Cell
- Pancreatic Cancer Cell Line
- Survivin Expression
- Focal Adhesion Kinase Expression
Pancreatic cancer is difficult to treat and patients have an overall 5-year survival rate of <5% and a median overall survival of <6 months [1, 2]. Many tumors are already unresectable at diagnosis due to metastasis or the presence of locally advanced disease, and thus the majority of patients are potential candidates for palliative treatment including chemotherapy . Gemcitabine (Gem) is currently the first line drug in the treatment of advanced pancreatic cancer [4, 5]. However, due to high intrinsic resistance of pancreatic cancer to currently available agents, clinical trials have shown that Gem alone and Gem-based combination chemotherapy are not likely to achieve great success [3, 4, 6]. Therefore, new therapeutic strategies are urgently needed. In pancreatic cancer, a combination of conventional chemotherapies with new therapies directly targeted against the molecular changes in pancreatic cancer seems to be the most promising strategy so far [7–9]. Tyrosine kinases have demonstrated great promise as therapeutic targets for cancers, and combinations of appropriate tyrosine kinase inhibitors (TKIs) with cytotoxic agents such as Gem have been demonstrated to improve the prognosis of pancreatic cancer [7, 10, 11]. Non-receptor tyrosine kinase focal adhesion kinase (FAK) has been shown to be closely related to cancers. FAK expression and (or) phosphorylation was elevated in a variety of cancers and frequently correlated with malignant or metastatic disease and poor patient prognosis [12, 13]. Moreover, the modulation of FAK expression and (or) phosphorylation influences the sensitivity of tumor cells to various chemotherapeutic agents, and combination of the selective FAK inhibitors with cytotoxic agents might be a very promising anti-cancer therapy [14–16]. High FAK protein expression is also present in pancreatic cancer, but not significantly related to clinicopathological factors such as tumor histological grade, lymph node metastasis, distant metastasis, histological stage, and overall survival in pancreatic cancer patients . Besides the regulation of FAK expression, another well-understood mode of FAK regulation in cancer cells is phosphorylation, particularly tyrosine phosphorylation . In this study, we first investigated the correlation between the level of constitutive FAK expression and phosphorylation and the extent of chemoresistance in four pancreatic cancer cell lines.
As we know, RNAi downregulates protein expression and thus activity. However, FAK related non-kinase (FRNK) can compete with FAK for focal adhesion binding sites and thus specifically inhibit FAK phosphorylation and downstream signaling without changing expression [19–21]. In our study, we used the two kinds of plasmids (FAK RNAi plasmid and FRNK overexpression plasmid) to further dissect the role of constitutive FAK phosphorylation in the chemoresistance of pancreatic cancer cells that had high level of pFAK.
Recently, a novel small molecule inhibitor, PF-573,228 (here after referred to as PF-228), has been developed to block FAK phosphorylation on Tyr397 and target FAK catalytic activity, which provides an appropriate tool to dissect the role of FAK phosphorylation . Compared with FRNK overexpression, PF-228 is a more specific method to decrease FAK phosphorylation. Therefore, PF-228 was used in our study to confirm the role of FAK phosphorylation in the chemoresistance of pancreatic cancer cells.
FAK is a key molecule in signal transduction from extracellular matrix (ECM) to cells, and it has been reported in recent years that the intrinsic chemoresistance of tumor cells could be induced by ECM-integrin interactions, named cell adhesion-mediated drug resistance (CAM-DR) . Laminin (LN) has been confirmed to be one of the most effective ECM proteins to induce CAM-DR [24–26]. Thus we further explored the role of LN on FAK phosphorylation and the intrinsic chemoresistance in the pancreatic cell line with low level of constitutive FAK phosphorylation.
Antibodies and reagents
Rabbit polyclonal antibodies to pERK1/2, ERK1/2, pAkt(pS473), AKT, pBad(pS112), pBad(pS136) and Bad were from Cell Signaling Technology (Beverly, MA, USA). Mouse monoclonal antibody (mAb) to pFAK (pY397) was purchased from BD Biosciences PharMingen (San Diego, CA, USA). FAK and FRNK (the carboxyl terminus of FAK) proteins, were detected by mAb raised against amino acids 903-1052 of human-origin FAK (Santa Cruz Biotechnology, Santa Cruz, CA, USA). Anti-β-actin, anti-Bcl-2, anti-Bax, anti-survivin, anti-caspase-3 primary antibodies and HRP-conjugated secondary antibodies were all purchased from Santa Cruz.
Gem was purchased from Eli Lilly (Indianapolis, IN, USA). 5-Fluorouracil (5-FU), MTT, insulin, transferrin, selenium, BSA and LN were all supplied by Sigma-Aldrich Chemical (Poole, UK). The FAK inhibitor PF-573,228 was purchased from Tocris (Bristol, UK).
Cell culture, transfection and generation of stable clones
Pancreatic cancer cell lines were all purchased from ATCC (Rockville, MD, USA). AsPC-1, Panc-1 and BxPC-3 were grown in RPMI 1640 (Invitrogen, Carlsbad, CA, USA) supplemented with 10% (v/v) heat-inactivated fetal calf serum (Gemini Bio-Products, Woodland, CA, USA), whereas MiaPaCa-2 cells were grown in DMEM. All cells were maintained at 37°C in a humidified atmosphere with 5% CO2. Cell viability was routinely checked after passage by trypan blue exclusion and was consistently >95%. In all experiments with Gem or 5-FU, cells were allowed to settle for 6 h prior to treatment.
Linearized pcDNA 6.2-GW/EmGFP-miR vector (Invitrogen) which enables increasing knockdown of a single target gene with one construct was used for vector-based RNAi interference (RNAi) analysis. This vector can express microRNA for RNAi analysis in most mammalian cells using the human cytomegalovirus immediate early promoter. Criteria for the selection of the target sequence were as we described previously . Plasmid construction was performed following the manufacturer's instructions. The RNAi vectors (FAK RNAi1, FAK RNAi2) were generated by ligating the annealed DNA oligos into the linearized vector and used to inhibit human FAK gene (GenBank: NM_153831.2). The control vector pcDNA 6.2-GW/EmGFP-miR-neg encodes an mRNA not to target any known vertebrate gene. The annealed oligos in FAK RNAi1 plasmid were:
5'TGCTGAGAAATTTCTCTCTCACGCTGGTTTTGGCCACTGACTGACCAGCGTGAGAGAAATTTCT3' (top strand)
5'CCTGAGAAATTTCTCTCACGCTGGTCAGTCAGTGGCCAAAACCAGCGTGAGAGAGAAATTTCTC3' (bottom strand).
The annealed oligos in FAK RNAi2 plasmid were:
5'TGCTGTTCACCTTCTTTCTGAGGTCTGTTTTGGCCACTGACTGACAGACCTCAAAGAAGGTGAA 3' (top strand)
5'CCTGTTCACCTTCTTTGAGGTCTGTCAGTCAGTGGCCAAAACAGACCTCAGAAAGAAGGTGAAC 3' (bottom strand).
FRNK was PCR amplified from the pRKvsv-FRNK plasmid that was kindly provided by Dr. Kenneth M. Yamada (National Institutes of Health, Bethesda, MD, USA) using the following forward and reverse primers:
5'TCCGGATCCATGGAATCCAGAAGACAGGCTAC 3' and 5'CCGGAATTCTCAGTGTGGCCGTGTCTGCCCTA3'. The PCR products were digested with BamHI and EcoRI and cloned into pcDNA3.1 to generate pcDNA3.1-FRNK plasmid. Empty pcDNA3.1 plasmid was used as control.
Cells were transiently transfected using Lipofectamine2000 reagent (Invitrogen) as suggested by the manufacturer. Stable clones were selected for blasticidin (pcDNA 6.2-GW/EmGFP-miR) or G418 (pcDNA3.1) resistance using standard protocols . Pools of four individual clones were used to avoid artifacts. Parental cells and pools transfected with vector plasmids were used as controls. G418 or blasticidin was removed from the culture media 24 h before functional assays.
Culture of cells on LN
Cell culture plastics were coated with LN (10 μg/cm2) for 2 h at 37°C. LN-coated dishes were rinsed three times with PBS. In all experiments using LN, cells were serum starved for 24 h before the experiments were performed. Cells were then distributed onto LN-coated (LN) or control (plastic) wells and cultured in SITA medium (RPMI 1640 supplemented with 30 nM selenium, 5 μg/ml insulin, 10 μg/ml transferrin, 0.25% (w/v) BSA, 100 U/ml penicillin and 100 μg/ml streptomycin).
Cells were treated as specified and then lysated in RIPA buffer (Pierce Biotechnology, Rockford, IL, USA) with protease inhibitor mixture tablets and phosphatase inhibitor mixture tablets PhosSTOP (Roche Applied Science, Mannheim, Germany). Protein concentration was determined by the BCA assay (Pierce). The whole-cell lysates were heat denatured at 100°C for 10 min before being run on 8-12% gradient SDS-PAGE. After SDS-PAGE, the proteins were electrotransferred onto nitrocellulosemembranes, blotted with each primary antibody, incubated in secondary antibody and then detected with enhanced chemiluminescence reagent (Amersham Pharmacia Biotech, Bucks, UK) and BioMax MR-1 radiographic film (Kodak, Xiamen, China). Semi-quantitative analysis of band intensities was performed by densitometry using image analysis software Image Pro-Plus (Media Cybernetics, Silver Spring, MD, USA).
Cells were grown on glass coverslips and fixed with 4% paraformaldehyde for 20 min at room temperature. Fixed cells were then incubated with the primary anti- pFAK (pY397) antibodies overnight, washed with PBS, and incubated again with secondary antibodies conjugated with FITC (green) for 1 h at room temperature. Hoechst 33342 was used to stain the nuclei (blue). Cells incubated with secondary antibodies alone were used as controls. The coverslips were mounted onto slides and cells were viewed by a Leica TCS-SP2 confocal scanning microscope (Leica Microsystems Heidelberg GmbH, Germany).
Cell viability assay
Cell viability was determined by MTT assay. Logarithmically growing cells were plated at 5 × 103 per well in 96-well plates and allowed to adhere for 6 h. The cells were then cultured in the absence or presence of different concentrations of 5-FU or Gem for the indicated time as specified in the Results. After treatment, 10 μL of the MTT was added to each well to assess the cell viability, and after 4 h at 37°C, the purple-blue MTT formazan precipitate was dissolved in 100 μl of DMSO, and the optical density was measured at 570 nm with a Vmax microplated spectrophotometer (Molecular Devices, Sunnyvale, CA). Each experiment was repeated at least thrice in quadruplicate. The concentration of Gem required to inhibit cell proliferation by 50% (IC50) was calculated using Microsoft Excel software for semi-log curve fitting with regression analysis.
Colony formation was evaluated using a soft agar clonogenic-forming assay. A volume of 0.5 ml of RPMI1640 containing 10% fetal bovine serum and 0.5% agar was plated on the bottom of 24-well plates. The plates were stored at 4°C to allow the agar to freeze. Cells were treated as specified in the Results, mixed with RPMI1640 containing 10% fetal bovine serum and 0.35% agar and plated onto the 24-well plates that were prepared earlier at 500 cells per well (three wells per group). The plates were then transferred to 37°C. After 14-18 days, colonies were manually counted using a microscope and also visualized by MTT stain.
Analysis of apoptosis by nuclear morphology
Apoptosis was judged by nuclear condensation. Distilled slides were placed onto the surface of 6-well plates, and then coated or not with LN as described above. Cells were seeded onto the slides, allowed to settle for 6 h and then treated with or without Gem for the indicated time. After treatment, slides were washed with PBS, and cells were fixed with 4% polyformaldehyde for 10 min. The slides were washed again with PBS, and 0.1 ml of Hoechst 33342 at a concentration of 2 μg/ml was added to each slide and incubated in the dark at room temperature for 15 min. The slides were washed three times with PBS, and the cells were examined using a Motic fluorescence microscope and photographed.
Flow cytometric assay of apoptosis
Phosphatidylserine externalization was analyzed with Annexin-V-FITC/PI kit (BD) by a FACSCalibur flow cytometer (BD) for cell apoptosis according to the manufacturer's instructions.
Results were expressed as the mean ± SE, and statistical differences between groups in these assays were calculated using a Student's two-tailed t test. Significance was defined as P < 0.05 using a two-sided analysis.
The level of constitutive phosphorylation of FAK at Tyr397 correlates with the extent of intrinsic chemoresistance to Gem in pancreatic cancer cell lines
Taken together, these results suggested that constitutive FAK phosphorylation was positively correlated with the intrinsic chemoresistance to Gem in pancreatic cancer cells.
Both FAK RNAi and FRNK overexpression decrease the phosphorylation of FAK and Akt in Panc-1 cells
Individual clones and pools of Panc-1 cells transfected with FAK RNAi2, pcDNA3.1-FRNK were obtained and examined for total FAK and pFAK (pY397) expression. Results observed in the stable clones were similar to the transient transfection experiments (Fig. 3C-D). Akt and ERK1/2 are two key kinases that are downstream of FAK, and they are important for mediating cell survival. In accord with decreased pFAK (pY397) levels, Panc-1 cells stably transfected with either FAK RNAi2 or pcDNA3.1-FRNK plasmid showed decreased Akt phosphorylation. However, the levels of total Akt, total ERK1/2 and pERK1/2 were not affected. RT-PCR analysis also showed that FAK mRNA level was decreased in Panc-1 cells stably transfected with FAK RNAi2 (data not shown).
These results confirmed that both FAK RNAi and FRNK overexpression decreased the phosphorylation of FAK and downstream kinase Akt in Panc-1 cells. To avoid artifacts resulting from the use of single clones of transfected cells, a pool of four individual clones was used for further experiments.
Both FAK RNAi and FRNK overexpression enhance Gem-induced cytotoxicity and apoptosis in Panc-1 cells
These results clearly showed that, inhibition of constitutive FAK phosphorylation was sufficient to render Panc-1 cells more chemosensitive to Gem. It indicated that constitutive pFAK was at least partially responsible for Gem chemoresistance in pancreatic cancer lines and suggested that the mechanisms might be related to survivin expression and pBad (pS136) level.
LN induces the phosphorylation of FAK and its downstream kinase Akt in AsPC-1 cells
These results indicated that in AsPC-1 cells, LN induced FAK and Akt phosphorylation in a time-dependent manner, and LN-induced Akt phosphorylation was mediated by FAK activation.
LN suppresses Gem-induced cytotoxicity and apoptosis in AsPC-1 cells
Collectively, these findings suggested that LN might mediate the intrinsic chemoresistance to Gem in AsPC-1 cells.
Effects of FAK RNAi and FRNK overexpression on LN-mediated Gem chemoresistance in AsPC-1 cells
When cultured on LN, pool cells expressing FRNK demonstrated a significant increase in Gem-induced apoptosis, compared with parental cells and vector cells (P < 0.05) (Fig. 10A-C). However, FRNK overexpression did not significantly affect Gem-induced apoptosis in AsPC-1 cells on plastic (Fig. 10B). Moreover, inhibition of FAK phosphorylation by FRNK overexpression antagonized the effects of LN on survivin expression and Bad phosphorylation at Ser136 in AsPC-1 cells (Fig. 10D). Similar results were observed with FAK RNAi in AsPC-1 cells (data not shown). These results indicated that in AsPC-1 cells, LN-induced FAK phosphorylation mediated the intrinsic chemoresistance to Gem, and this effect might be related with the regulation of survivin and pBad (pS136) level
Effects of PF-228 on Gem-induced apoptosis in pancreatic cancer cells
PF-228, a novel FAK inhibitor, has become available recently. It specifically blocks FAK phosphorylation and thus targets FAK catalytic activity. PF-228 is a more specific method to decrease FAK phosphorylation compared with FRNK overexpression. Therefore, in our study PF-228 was further applied to confirm the role of FAK phosphorylation in the chemoresistance of pancreatic cancer cells.
These results further confirmed that, constitutive and LN-induced FAK phosphorylation was at least partially responsible for the intrinsic chemoresistance to Gem in pancreatic cancer cells.
Pancreatic cancer remains a major therapeutic challenge. High resistance to chemotherapy is considered a common phenomenon and one of the major reasons for poor prognosis in pancreatic cancer . Links between tyrosine kinases and tumor chemoresistance have attracted more and more attention in recent years . The combination of targeted therapy against tyrosine kinases and conventional approved drugs such as Gem has proven effective in both preclinical and clinical settings [8, 10, 11].
A pivotal role of the non-receptor tyrosine kinase FAK has been demonstrated in a variety of human tumors by immunohistochemical and molecular analysis. FAK expression or phosphorylation is elevated in ovarian, breast, head and neck, thyroid, esophageal, colon, liver and pancreatic cancers, indicating that FAK might be a novel therapeutic target and prognostic marker for these malignancies [12, 13, 17, 23]. Consistent with a previous study , all four pancreatic cancer cell lines that we tested showed high FAK expression at the protein level. In recent studies, researchers have begun to hypothesize that FAK is a key determinant of chemoresistance since the modulation of FAK function through antisense oligonucleotides or RNAi influences the sensitivity of different kinds of tumor cells to various chemotherapeutic agents [15, 16, 34]. Herein, we examined whether constitutive FAK protein expression in pancreatic cancer cells correlated with the intrinsic chemoresistance to Gem or 5-FU. However, our study showed total FAK protein expression which was similar among all four cell lines, did not correlate with Gem or 5-FU chemoresistance. It has also been reported previously that FAK protein expression might not be a prognostic marker for pancreatic cancer patients . Tyrosine 397 is the major site of autophosphorylation in FAK. Phosphorylation at Tyr397 correlates with increased catalytic activity of FAK and is important for tyrosine phosphorylation of focal-adhesion-associated proteins [35, 36]. Our study here showed that constitutive pFAK (pY397) levels positively correlated with Gem chemoresistance in pancreatic cancer cell lines. This indicates that the phosphorylated active form of FAK may be of greater biological significance compared with the total expression.
We demonstrated herein that specific RNAi against FAK reduced FAK expression, decreased FAK phosphorylation and thus suppressed the intrinsic chemoresistance to Gem in Panc-1 cells, which had a high level of pFAK (pY397). Our results indicate that FAK is a potential target for pancreatic cancer treatment. The C-terminal non-catalytic domain of FAK termed FRNK functions as a competitive inhibitor of FAK and ectopic expression of FRNK specifically inhibits FAK autophosphorylation at Tyr397 and thus attenuates its activity [19, 20]. In our study, FRNK overexpression enhanced Gem-induced cytotoxicity and apoptosis to a similar extent as FAK RNAi in Panc-1 cells. However, FRNK overexpression did not significantly affect Gem-induced apoptosis in AsPC-1 cells that had low level of pFAK (pY397). These results demonstrate that constitutive FAK phosphorylation contributes to the intrinsic chemoresistance to Gem in pancreatic cancer cells. Previous study in breast cancer cells has also found that FRNK overexpression inhibited the activation of FAK and PKB and thus enhanced chemotherapy-induced cell apoptosis . Small molecule inhibitors of FAK phosphorylation (such as PF-573,228, PF-562,271, TAE226, 1,2,4,5-Benzenetetraamine tetrahydrochloride) have been developed in recent years [22, 38–40]. PF-562,271 is a potent inhibitor of both FAK and the related kinase Pyk2, while TAE226 is an effective inhibitor of both FAK and insulin-like growth factor I receptor . Therefore, a commercially available and more specific inhibitor of FAK phosphorylation, PF-228, was chosen in our study. Compared with FRNK, PF-228 can more specifically block FAK autophosphorylation both in normal and tumor cells. As expected, inhibition of constitutive FAK phosphorylation by PF-228 also decreased the intrinsic chemoresistance to Gem in Panc-1 cells. It further confirms the role of constitutive FAK phosphorylation in the intrinsic chemoresistance to Gem in pancreatic cancer cells and indicates development of selective FAK phosphorylation inhibitors may be a promising way to enhance chemosensitivity in pancreatic cancer. Interestingly, FRNK overexpression or PF-228 alone did not induce apoptosis in pancreatic cancer cells. Consistent with this, a previous study reported that PF-228 had no effect on the growth or apoptosis of normal or cancer cells .
In recent years, ECM proteins such as LN, fibronectin and collagen I have been thought to be associated with the intrinsic chemoresistance of many cancers. This phenomenon called CAM-DR represents a novel intrinsic pathway for evading drug-induced apoptosis [23, 25, 26, 41]. Previous data have also shown that α6β1 integrins, major LN-binding receptor, are highly expressed in pancreatic cancer tissues and cell lines, including AsPC-1 [25, 42]. Our study demonstrated that LN preventedAsPC-1 cells from Gem-induced cytotoxicity and apoptosis. It indicates that CAM-DR might be an important intrinsic chemoresistance mechanism in pancreatic cancer. Moreover, it has also been reported that Type I collagen reduced apoptosis of AsPC-1 cells in response to 5-FU . FAK functions as a critical intracellular mediator in the ECM-integrin-initiated signaling pathway [44, 45]. Our studies found that LN induced FAK phosphorylation in a time-dependent manner in AsPC-1 cells, and FAK phosphorylation inhibition by either RNAi or FRNK overexpression antagonized the effect of LN on Gem chemoresistance. The role of LN-induced FAK phosphorylation in LN-mediated Gem chemoresistance was further confirmed by using the more specific inhibitor of FAK phosphorylation, PF-228. These results indicate that induced FAK phosphorylation is involved in LN-mediated chemoresistance to Gem and further confirm FAK as a promising therapeutic target in pancreatic cancer. Targeted therapy against FAK by methods such as using specific phosphorylation inhibitors could potentially be used to inhibit the cell-ECM interaction and thus suppress CAM-DR.
Akt and ERK are key downstream effectors of FAK in mediating cell survival [44, 46, 47]. Upon integrin binding to ECM or other stimuli, FAK is autophosphorylated at Tyr397, which provides a high-affinity docking site for several proteins including the p85 subunit of PI3K and the Src kinase. Src can further phosphorylate FAK at several additional sites, including Tyr925. The phosphorylation of Tyr397, as well as of Tyr925, creates a binding site for the Grb2-SOS complex which then permits signaling to the RAS-MAPK cascade . Our research showed that specific inhibition of constitutive FAK phosphorylation decreased Akt but not ERK phosphorylation in Panc-1 cells. Similarly, in Aspc-1 cells, LN-induced FAK phosphorylation was accompanied by Akt but not ERK activation, and specific inhibition of FAK phosphorylation decreased LN-induced Akt activation. These data indicate that Akt might be involved in the intrinsic chemoresistance mediated by FAK phosphorylation. These results are supported by previous reports that the PI-3K-Akt pathway was responsible for Gem chemoresistance in pancreatic cancer in vivo and in vitro. Moreover, PI-3K-Akt has also been shown to be involved in CAM-DR in small cell lung cancer [26, 48].
Apoptosis-associated proteins have been reported to relate with chemoresistance in malignant tumors including pancreatic cancers [29–32]. Pro-apoptosis protein Bad is modulated by phosphorylation at two sites, Ser112 (ERK-dependent) and Ser136 (Akt-dependent). Phosphorylation prevents Bad from binding either Bcl-2 or Bcl-XL and thus suppresses apoptosis. Inhibition of phosphorylation at either site might sensitize tumor cells to chemotherapy [31, 49]. In our study, corresponding with the alteration of Akt, pBad (pS136) was regulated by constitutive and induced FAK phosphorylation in pancreatic cancer cells. In addition, survivin exression was also regulated by FAK phosphorylation. These data imply that pBad and survivin might contribute to the intrinsic chemoresistance mediated by constitutive and LN-induced FAK phosphorylation.
Our research demonstrates for the first time that both constitutive and LN-induced phosphorylation of FAK contribute to the intrinsic chemoresistance to Gem in pancreatic cancer cell lines. This effect may be partially due to the regulation of Akt signaling pathway and apoptosis-associated proteins. Our results suggest that FAK can be an attractive therapeutic target for pancreatic cancer, and the development of selective FAK phosphorylation inhibitors may be a promising way to enhance Gem chemosensitivity in pancreatic cancer.
This study was supported by a grant 2006BAI02A14 of 11th Five-Year Plan scientific and technological support from the Ministry of Science and Technology of the Peoples' Republic of China.
- Jemal A, Siegel R, Ward E, Hao Y, Xu J, Murray T, Thun MJ: Cancer statistics, 2008. CA Cancer J Clin. 2008, 58: 71-96. 10.3322/CA.2007.0010View ArticlePubMedGoogle Scholar
- Li D, Xie K, Wolff R, Abbruzzese JL: Pancreatic cancer. Lancet. 2004, 363: 1049-57. 10.1016/S0140-6736(04)15841-8View ArticlePubMedGoogle Scholar
- von Wichert G, Seufferlein T, Adler G: Palliative treatment of pancreatic cancer. J Dig Dis. 2008, 9: 1-7. 10.1111/j.1443-9573.2007.00314.xView ArticlePubMedGoogle Scholar
- O'Reilly EM, Abou-Alfa GK: Cytotoxic therapy for advanced pancreatic adenocarcinoma. Semin Oncol. 2007, 34: 347-53. 10.1053/j.seminoncol.2007.05.009View ArticlePubMedGoogle Scholar
- Xiong HQ, Carr K, Abbruzzese JL: Cytotoxic chemotherapy for pancreatic cancer: Advances to date and future directions. Drugs. 2006, 66: 1059-72. 10.2165/00003495-200666080-00003View ArticlePubMedGoogle Scholar
- Burris H, Rocha-Lima C: New therapeutic directions for advanced pancreatic cancer: targeting the epidermal growth factor and vascular endothelial growth factor pathways. Oncologist. 2008, 13: 289-98. 10.1634/theoncologist.2007-0134View ArticlePubMedGoogle Scholar
- Kleespies A, Jauch KW, Bruns CJ: Tyrosine kinase inhibitors and gemcitabine: new treatment options in pancreatic cancer?. Drug Resist Updat. 2006, 9: 1-18. 10.1016/j.drup.2006.02.002View ArticlePubMedGoogle Scholar
- Danovi SA, Wong HH, Lemoine NR: argeted therapies for pancreatic cancer. Br Med Bull. 2008, 87: T97-130. 10.1093/bmb/ldn027.View ArticleGoogle Scholar
- Ko AH: Future strategies for targeted therapies and tailored patient management in pancreatic cancer. Semin Oncol. 2007, 34: 354-64. 10.1053/j.seminoncol.2007.05.002View ArticlePubMedGoogle Scholar
- Borja-Cacho D, Jensen EH, Saluja AK, Buchsbaum DJ, Vickers SM: Molecular targeted therapies for pancreatic cancer. Am J Surg. 2008, 196: 430-41. 10.1016/j.amjsurg.2008.04.009PubMed CentralView ArticlePubMedGoogle Scholar
- Moore MJ, Goldstein D, Hamm J, Figer A, Hecht JR, Gallinger S, Au HJ, Murawa P, Walde D, Wolff RA: Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol. 2007, 25: 1960-6. 10.1200/JCO.2006.07.9525View ArticlePubMedGoogle Scholar
- de Heer P, Koudijs MM, Velde van de CJ, Aalbers RI, Tollenaar RA, Putter H, Morreau J, Water van de B, Kuppen PJ: Combined expression of the non-receptor protein tyrosine kinases FAK and Src in primary colorectal cancer is associated with tumor recurrence and metastasis formation. Eur J Surg Oncol. 2008, 34: 1253-61.View ArticlePubMedGoogle Scholar
- Chatzizacharias NA, Kouraklis GP, Theocharis SE: Clinical significance of FAK expression in human neoplasia. Histol Histopathol. 2008, 23: 629-50.PubMedGoogle Scholar
- van Nimwegen MJ, Water van de B: Focal adhesion kinase: a potential target in cancer therapy. Biochem Pharmacol. 2007, 73: 597-609. 10.1016/j.bcp.2006.08.011View ArticlePubMedGoogle Scholar
- Halder J, Kamat AA, Landen CN, Han LY, Lutgendorf SK, Lin YG, Merritt WM, Jennings NB, Chavez-Reyes A, Coleman RL: Focal adhesion kinase targeting using in vivo short interfering RNA delivery in neutral liposomes for ovarian carcinoma therapy. Clin Cancer Res. 2006, 12: 4916-24. 10.1158/1078-0432.CCR-06-0021PubMed CentralView ArticlePubMedGoogle Scholar
- Smith CS, Golubovskaya VM, Peck E, Xu LH, Monia BP, Yang X, Cance WG: Effect of focal adhesion kinase (FAK) downregulation with FAK antisense oligonucleotides and 5-fluorouracil on the viability of melanoma cell lines. Melanoma Res. 2005, 15: 357-62. 10.1097/00008390-200510000-00003View ArticlePubMedGoogle Scholar
- Furuyama K, Doi R, Mori T, Toyoda E, Toyoda E, Ito D, Kami K, Koizumi M, Kida A, Kawaguchi Y, Fujimoto K: Clinical significance of focal adhesion kinase in resectable pancreatic cancer. World J Surg. 2006, 30: 219-26. 10.1007/s00268-005-0165-zView ArticlePubMedGoogle Scholar
- McLean GW, Carragher NO, Avizienyte E, Evans J, Brunton VG, Frame MC: The role of focal-adhesion kinase in cancer - a new therapeutic opportunity. Nat Rev Cancer. 2005, 5: 505-15. 10.1038/nrc1647View ArticlePubMedGoogle Scholar
- Richardson A, Parsons T: A mechanism for regulation of the adhesion-associated prote in tyrosine kinase pp125FAK. Nature. 1996, 380: 538-40. 10.1038/380538a0View ArticlePubMedGoogle Scholar
- Walker HA, Whitelock JM, Garl PJ, Nemenoff RA, Stenmark KR, Weiser-Evans MC: Perlecan up-regulation of FRNK suppresses smooth muscle cell proliferation via inhibition of FAK signaling. Mol Biol Cell. 2003, 14: 1941-52. 10.1091/mbc.E02-08-0508PubMed CentralView ArticlePubMedGoogle Scholar
- Li S, Hua ZC: FAK expression regulation and therapeutic potential. Adv Cancer Res. 2008, 101: 45-61. 10.1016/S0065-230X(08)00403-XView ArticlePubMedGoogle Scholar
- Slack-Davis JK, Martin KH, Tilghman RW, Iwanicki M, Ung EJ, Autry C, Luzzio MJ, Cooper B, Kath JC, Roberts WG, Parson JT: Cellular characterization of a novel focal adhesion kinase inhibitor. J Biol Chem. 2007, 282: 14845-52. 10.1074/jbc.M606695200View ArticlePubMedGoogle Scholar
- Damiano JS, Cress AE, Hazlehurst LA, Shtil AA, Dalton WS: Cell adhesion mediated drug resistance (CAM-DR): role of integrins and resistance to apoptosis in human myeloma cell lines. Blood. 1999, 93: 1658-67.PubMedGoogle Scholar
- Cordes N: Integrin-mediated cell-matrix interactions for prosurvival and antiapoptotic signaling after genotoxic injury. Cancer Lett. 2006, 242: 11-9. 10.1016/j.canlet.2005.12.004View ArticlePubMedGoogle Scholar
- Miyamoto H, Murakami T, Tsuchida K, Sugino H, Miyake H, Tashiro S: Tumor-stroma interaction of human pancreatic cancer: acquired resistance to anticancer drugs and proliferation regulation is dependent on extracellular matrix proteins. Pancreas. 2004, 28: 38-44. 10.1097/00006676-200401000-00006View ArticlePubMedGoogle Scholar
- Hodkinson PS, Elliott T, Wong WS, Rintoul RC, Mackinnon AC, Haslett C, T Sethi: ECM overrides DNA damage-induced cell cycle arrest and apoptosis in small-cell lung cancer cells through beta1 integrin-dependent activation of PI3-kinase. Cell Death Differ. 2006, 13: 1776-88. 10.1038/sj.cdd.4401849View ArticlePubMedGoogle Scholar
- Shi XH, Liang ZY, Ren XY, Liu TH: Combined silencing of K-ras and Akt2 oncogenes achieves synergistic effects in inhibiting pancreatic cancer cell growth in vitro and in vivo. Cancer Gene Ther. 2009, 16: 227-36.PubMedGoogle Scholar
- Ricci MS, Zong WX: Chemotherapeutic approaches for targeting cell death pathways. Oncologist. 2006, 11: 342-57. 10.1634/theoncologist.11-4-342PubMed CentralView ArticlePubMedGoogle Scholar
- Xu ZW, Friess H, Buchler MW, Solioz M: Overexpression of Bax sensitizes human pancreatic cancer cells to apoptosis induced by chemotherapeutic agents. Cancer Chemother Pharmacol. 2002, 49: 504-10. 10.1007/s00280-002-0435-5View ArticlePubMedGoogle Scholar
- Shi X, Liu S, Kleeff J, Friess H, Buchler MW: Acquired resistance of pancreatic cancer cells towards 5-Fluorouracil and gemcitabine is associated with altered expression of apoptosis-regulating genes. Oncology. 2002, 62: 354-62. 10.1159/000065068View ArticlePubMedGoogle Scholar
- Hayakawa J, Ohmichi M, Kurachi H, Kanda Y, Hisamoto K, Nishio Y, Adachi K, Tasaka K, Kanzaki T, Murata Y: Inhibition of BAD phosphorylation either at serine 112 via extracellular signal-regulated protein kinase cascade or at serine 136 via Akt cascade sensitizes human ovarian cancer cells to cisplatin. Cancer Res. 2000, 60: 5988-94.PubMedGoogle Scholar
- Liu WS, Yan HJ, Qin RY, Liu WS, Yan HJ, Qin RY: siRNA directed against survivin enhances pancreatic cancer cell gemcitabine chemosensitivity. Dig Dis Sci. 2009, 54: 89-96. 10.1007/s10620-008-0329-4View ArticlePubMedGoogle Scholar
- Reddig PJ, Juliano RL: Clinging to life: cell to matrix adhesion and cell survival. Cancer Metastasis Rev. 2005, 24: 425-439. 10.1007/s10555-005-5134-3View ArticlePubMedGoogle Scholar
- Duxbury MS, Ito H, Benoit E, Zinner MJ, Ashley SW, Whang EE: RNA interference targeting focal adhesion kinase enhances pancreatic adenocarcinoma gemcitabine chemosensitivity. Biochem Biophys Res Commun. 2003, 311: 786-92. 10.1016/j.bbrc.2003.10.060View ArticlePubMedGoogle Scholar
- Parsons JT: Focal adhesion kinase: the first ten years. J Cell Sci. 2003, 116: 1409-16. 10.1242/jcs.00373View ArticlePubMedGoogle Scholar
- Mitra SK, Hanson DA, Schlaepfer DD: Focal adhesion kinase: in command and control of cell motility. Nat Rev Mol Cell Biol. 2005, 6: 56-68. 10.1038/nrm1549View ArticlePubMedGoogle Scholar
- van Nimwegen MJ, Huigsloot M, Camier A, Tijdens IB, Water van de B: Focal adhesion kinase and protein kinase B cooperate to suppress doxorubicin-induced apoptosis of breast tumor cells. Mol Pharmacol. 2006, 70: 1330-9. 10.1124/mol.106.026195View ArticlePubMedGoogle Scholar
- Parsons JT, Slack-Davis J, Tilghman R, Roberts WG: Focal adhesion kinase: targeting adhesion signaling pathways for therapeutic intervention. Clin Cancer Res. 2008, 14: 627-63. 10.1158/1078-0432.CCR-07-2220View ArticlePubMedGoogle Scholar
- Jones ML, Shawe-Taylor AJ, Williams CM, Poole : Characterization of a novel focal adhesion kinase inhibitor in human platelets. Biochem Biophys Res Commun. 2009, 389: 198-203. 10.1016/j.bbrc.2009.08.132PubMed CentralView ArticlePubMedGoogle Scholar
- Golubovskaya VM, Nyberg C, Zheng M, Kweh F, Magis A, Ostrov D, Cance WG: A small molecule inhibitor, 1, 2, 4, 5-benzenetetraamine tetrahydrochloride, targeting the y397 site of focal adhesion kinase decreases tumor growth. J Med Chem. 2008, 51: 7405-16. 10.1021/jm800483vPubMed CentralView ArticlePubMedGoogle Scholar
- Shain KH, Dalton WS: Cell adhesion is a key determinant in de novo multidrug resistance (MDR): new targets for the prevention of acquired MDR. Mol Cancer Ther. 2001, 1: 69-78.PubMedGoogle Scholar
- Lohr M, Trautmann B, Gottler M, Peters S, Zauner I, Maier A, Kloppel G, Liebe S, Kreuser ED: Expression and function of receptors for extracellular matrix proteins in human ductal adenocarcinomas of the pancreas. Pancreas. 1996, 12: 248-59. 10.1097/00006676-199604000-00007View ArticlePubMedGoogle Scholar
- Armstrong T, Packham G, Murphy LB, Bateman AC, Conti JA, Fine DR, Johnson CD, Benyon RC, Iredale JP: Type I collagen promotes the malignant phenotype of pancreatic ductal adenocarcinoma. Clin Cancer Res. 2004, 10: 7427-37. 10.1158/1078-0432.CCR-03-0825View ArticlePubMedGoogle Scholar
- Fong YC, Liu SC, Huang CY, Li TM, Hsu SF, Kao ST, Tsai FJ, Chen WC, Chen CY, Tang CH: Osteopontin increases lung cancer cells migration via activation of the alphavbeta3 integrin/FAK/Akt and NF-kappaB-dependent pathway. Lung Cancer. 2009, 64: 263-70. 10.1016/j.lungcan.2008.09.003View ArticlePubMedGoogle Scholar
- Bouchard V, Harnois C, Demers MJ, Vallee K, Gagne D, Fujita N, Tsuruo T, Vezina A, Beaulieu JF, Cote A, Vachon PH: B1 integrin/Fak/Src signaling in intestinal epithelial crypt cell survival: integration of complex regulatory mechanisms. Apoptosis. 2008, 13: 531-42. 10.1007/s10495-008-0192-yView ArticlePubMedGoogle Scholar
- Bouchard V, Demers MJ, Thibodeau S, Laquerre V, Fujita N, Tsuruo T, Beaulieu JF, Gauthier R, Vezina A, Villeneuve L, Vachon PH: Fak/Src signaling in human intestinal epithelial cell survival and anoikis: differentiation state-specific uncoupling with the PI3-K/Akt-1 and MEK/Erk pathways. J Cell Physiol. 2007, 212: 717-28. 10.1002/jcp.21096View ArticlePubMedGoogle Scholar
- Liao CH, Sang S, Ho CT, Lin JK: Garcinol modulates tyrosine phosphorylation of FAK and subsequently induces apoptosis through down-regulation of Src, ERK, and Akt survival signaling in human colon cancer cells. J Cell Biochem. 2005, 96: 155-69. 10.1002/jcb.20540View ArticlePubMedGoogle Scholar
- Tsurutani J, West KA, Sayyah J, Gills JJ, Dennis PA: Inhibition of the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin pathway but not the MEK/ERK pathway attenuates laminin-mediated small cell lung cancer cellular survival and resistance to imatinib mesylate or chemotherapy. Cancer Res. 2005, 65: 8423-32. 10.1158/0008-5472.CAN-05-0058View ArticlePubMedGoogle Scholar
- Mabuchi S, Ohmichi M, Kimura A, Hisamoto K, Murata Y: Inhibition of phosphorylation of BAD and Raf-1 by Akt sensitizes human ovarian cancer cells to paclitaxel. J Biol Chem. 2002, 277: 33490-500. 10.1074/jbc.M204042200View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.