Tissue transglutaminase-induced alterations in extracellular matrix inhibit tumor invasion
© Mangala et al; licensee BioMed Central Ltd. 2005
Received: 13 July 2005
Accepted: 09 September 2005
Published: 09 September 2005
Alterations in the extracellular matrix (ECM) can affect host-tumor interactions and tumor growth and metastasis. Tissue transglutaminase (TG2, EC 126.96.36.199), a calcium-dependent enzyme that catalyzes covalent cross-linking of proteins, can render the ECM highly stable and resistant to proteolytic degradation. So we determined whether TG2 expression in a tumor or nontumor (stroma) environment could affect the process of metastasis. Two hundred archived samples from patients with breast cancer were studied for the TG2 expression. Also, in an in vitro model the invasive behavior of MDA-MB-231 cells in the presence or absence of exogenous TG2 was determined.
Tumors associated with negative nodes showed significantly higher expression of TG2 in the stroma (P < 0.001). TG2 in the stroma was catalytically active, as revealed by the presence of isopeptide cross-links. Pretreatment of Matrigel with catalytically active TG2 resulted in strong inhibition of invasion of MDA-MB-231 cells through the Matrigel Transwell filters.
TG2-induced alterations in the ECM could effectively inhibit the process of metastasis. Therefore, selective induction of catalytically active TG2 at the site of tumor may offer promising approach for limiting the metastasis.
Despite significant advances in the treatment of primary breast cancer, predicting and preventing metastasis remains a daunting clinical challenge. To make progress in this area, it is imperative to understand the molecular mechanisms that regulate the progression from a primary tumor to metastatic disease.
Metastasis is a multistep process that involves intravasation, adhesion to a blood vessel wall, extravasation, infiltration, and the proliferation of cancer cells in the target tissue . Many of these steps require interaction between tumor cells and the extracellular matrix (ECM). For example, the ECM can modulate tumor cell growth by binding to and storing cytokines, it can promote cell attachment and migration by providing a stable foundation, and it can support cell growth and survival by interacting with cell-surface receptors and activating appropriate signaling pathways [2, 3].
Several lines of evidence have suggested that tissue transglutaminase (TG2, EC 188.8.131.52) plays an important role in stabilizing the ECM by cross-linking its component proteins and rendering it resistant to mechanical and proteolytic degradation [4–7]. TG2, a member of the Ca2+-dependent family of mammalian enzymes, catalyzes irreversible cross-linking of proteins by inserting highly stable ε(γ-glutamyl)lysine bonds between them [5, 8, 9]. Several ECM proteins, such as fibronectin, vitronectin, collagen, fibrin, laminin, osteonectin, and osteopontin, can serve as substrates in TG2-catalyzed cross-linking reactions [4, 10–12]. Moreover, in various fibrotic disorders, such as pulmonary fibrosis, renal fibrosis, and atherosclerosis increased expression of TG2 has been observed, and its ability to cross-link ECM proteins has been implicated in facilitating the deposition of a new ECM and making it resistant to metalloproteinases [12–16]. In addition to its direct role in promoting the accumulation of the ECM, TG2 has been implicated in the storage and activation of transforming growth factor-beta (TGF-β) , a proinflammatory cytokine that is involved in the synthesis of various ECM proteins and inhibitors of metalloproteinases [18, 19]. The ability of TG2 to affect the physicochemical properties of the ECM may influence the invasive properties of tumor cells by modulating cell-matrix interactions or by facilitating the assembly of the matrix and tissue remodeling.
In view of these facts and other observations that modification of the ECM can affect the growth of both normal and cancerous mammary epithelial cells and the processes of angiogenesis and tumor metastasis [20–22], we speculated that TG2 expression in the stroma of the host can affect breast cancer progression. To test this theory, we searched for such a correlation in tumor and stroma specimens in a total 200 samples from patients with early-stage breast cancer. Our findings suggested that TG2 expression in the stroma was associated with an absence of lymph node metastasis in patients with breast cancer. The results of our in vitro study further supported this link and suggested that TG2-mediated modification of the ECM could render it less susceptible to invasion by tumor cells. Taken together, these findings suggest that TG2 is a good candidate for therapeutic use to prevent progression from a primary tumor to metastatic disease in patients with breast cancer.
TG2 expression in tumor and stroma tissues of patients with breast cancer
TG2 in tumor
TG2 in stroma
The association of TG2 expression in tumors and stroma with node-negative or -positive status is presented in Table 1. There was no evidence that TG2 expression in tumor cells differed between node-negative or node-positive samples. Nevertheless, there was strong evidence that tumors associated with negative nodes had a significantly higher TG2 expression in the stroma (P < 0.001). With regard to the association of TG2 expression in tumors and stroma with age, there was no evidence of a difference in younger (<50 yrs) or older (>50 yrs) patient populations.
Major findings to emerge from this study are: in some patients with breast cancer, tumor and nontumor (stroma) environments express increased levels of TG2; in the stroma, TG2 protein exists in a catalytically active configuration, leading to cross-linking of the ECM proteins; and TG2-catalyzed cross-linking of ECM proteins may mitigate the migration of cancer cells to distant sites.
TG2 is a multifunctional protein that can affect the ECM and its interaction with cells. Both the extracellular cross-linking and intracellular signaling activities of TG2 can considerably modulate cell-matrix interactions . We previously observed that TG2 expression was up-regulated in drug-resistant and metastatic breast cancer cells and cell lines [23–28]. The increased expression of TG2 in drug-resistant and metastatic breast cancer cells was linked to their increased resistance to apoptosis, owing to the fact that TG2 in these cells closely associates with β integrins and thus may promote cell survival signaling [28–30]. The primary objective of this study was to determine whether higher levels of TG2 in breast cancer cells were associated with node involvement and development of aggressive tumors. We found no evidence that TG2 tumor staining differed between tumor samples associated with negative or positive node status. These results are in agreement with those of a previous study that revealed a negative correlation between TG2 transcript expression and nodal status in patients with breast cancer . However, in another report, Jiang et al. observed that lymph node involvement and development of aggressive phenotype in breast cancer tumors was associated with increased expression of TG2 transcript and decreased levels of TG3 and TG7 transcript expression . Similarly, another group has reported a marked increase in TG2 expression in the intraductal and invasive human breast cancer cells . Taken together, these observations suggest that transglutaminases' repertoire is altered during breast cancer development and progression. Therefore, further studies are warranted with larger cohort of patients to determine the prognostic significance of transglutaminases in the progression and development of metastatic disease in patients with breast cancer.
More important, the results of our study suggest that TG2 expression in the stroma is strongly associated with node-negative status in patients with breast cancer. A similar increase in TG2 expression in the stroma surrounding the tumor was observed by Haroon et al. in subcutaneously implanted rat mammary tumors . Treatment of these tumors with enzymatically active TG2 significantly delayed the tumor growth when compared with the tumors treated with catalytically inactive TG2 mutant. On the basis of these observations the authors concluded that TG2 might constitute a distinct part of the host response against growing tumor and by crosslinking the component proteins, it may stabilize the ECM and affect the tumor growth .
It is possible that local injury caused by the growing tumor may elicit host's response and induce cytokines production that in turn may promote wound healing and restrict the invasion of cells by producing new or stable ECM . Indeed, TG2 is capable of cross-linking several constituent proteins in the ECM, which can render the ECM more resistant to proteases and mechanical disruptions [4–6]. TG2 can also enhance stability and strengthen the ECM by its ability to facilitate the activation of tumor growth factor-beta . Thus, TG2-mediated alterations may render the ECM more amenable to tumor growth and resistant to proteases [36–38]. Indeed, our in vitro data shown in figure 2 clearly supported this contention and suggested that TG2-mediated crosslinking of component proteins rendered the matrigel resistant to invasion by MDA-MB-231 cells regardless of the fact that these cells actively produced matrix metalloproteinases (MMP) such as MMP-1 and MMP-2.
In conclusion, our findings suggest that increased expression of TG2 in the stroma represents a part of the host response to a growing tumor in an attempt to restrict tumor growth and prevent it from spreading to distant sites. However, the ability of tumor cells to produce proteases and other factors that could render TG2 inactive may overwhelm the ability of TG2 to inhibit growth and prevent metastasis. Indeed, TG2 has been shown to be a good substrate for MMP-2-like proteases that are abundantly produced by metastatic tumors [39, 40]. Future studies to selectively enhance the production of active TG2 at the site of tumor growth may offer promising approaches to limiting tumor growth and metastasis.
Cell Lines and Tumor Tissues
Human breast cancer cell line MDA-MB-231 was purchased from American Type Culture Collection (Rockville, MD) and cultured by standard methods. Tumor samples from 200 patients with early-stage breast cancer diagnosed between 1979 and 2002 were obtained from the archives of the Pathology Department of The University of Texas M. D. Anderson Cancer Center after approval by the Institutional Review Board for the Welfare of Human Subjects. All the selected patients had tumors ranging from 1 cm to 2 cm in largest diameter. Samples were selected for inclusion to yield 100 tumor samples that were associated with lymph node invasion and 100 tumor samples that were not associated with lymph node invasion.
The invasive behavior of MDA-MB-231 cells in the presence or absence of exogenous TG2 was determined in vitro by counting how many cells invaded through Matrigel-coated Transwell polycarbonate membrane inserts, as described previously [41, 42]. Briefly, Transwell inserts with a pore size of 12 μm were coated with 0.78 mg/ml Matrigel in cold, serum-free medium. In some cases, the Matrigel was preincubated (37°C for 15 minutes) with varying concentrations of purified TG2 protein (Sigma-Aldrich Chemical Co., St. Louis, MO) in the presence or absence of 5 mM Ca2+ before being coated onto the inserts. Also, Matrigel samples (40 μl aliquots) pretreated with varying concentrations of TG2 in the presence or absence of Ca2+ were subjected to 7% SDS-PAGE. The gel was stained with Coomassie brilliant blue and destained in a acetic acid and methanol solution before visualizing the changes in protein bands as a consequence of TG2-mediated crosslinking.
Cells were recovered by trypsinization and washed once with serum-free medium. The cell pellets were resuspended in serum-free medium, and 0.5 ml of the cell suspension (0.5 × 106 cells) was added to duplicate wells. After incubation for 48 hours, the cells that passed through the filter were stained using a Hema-3 stain kit (Fisher Scientific, Houston, TX), and the cells in 10 random fields were counted under a microscope.
Matrix Metalloproteinases (MMP)
Basal expression of MMP-1 and MMP-2 in MDA-MB-231 cells was determined by gelatin-substrate gel zymography as described . Briefly, the supernatant from MDA-MB-231 cultured cells was subjected under nonreducing conditions to gelatin impregnated (0.1%; w/v) SDS-PAGE. The gel was washed several times to remove the SDS and incubated in buffer containing 5 mM CaCl2 plus 1 μM ZnCl2 for 24–48 h at 37°C. The gel was stained with Coomassie brilliant blue and destained. Proteolytic activity was visualized as clear bands (zones of gelatin degradation) against the blue background of stained gelatin.
For RT-PCR, total RNA was isolated from MDA-MB-231 cells in Trizol reagent (Invitrogen, Life technologies, CA) and cDNA was synthesized from 5 μg of total RNA using Superscript reverse transcriptase (Life Technologies, Inc) as per the manufacturer's instructions. cDNA was subjected to PCR (GeneAmp PCR System 9700, Applied Biosystems) using MMP-1 specific, 5'-CGACTCTAGAAACACAAGAGCAAGA-3' (sense) and 5'-AAGGTTAGCTTACTGTCACACGCTT-3'(antisense) primers. PCR consisted of 30 cycles was carried out at the following conditions: 95°C for 5 min, 30 cycles of 95°C for 30 sec, annealing at 58°C for 1 min and elongation at 72°C for 2 min. PCR products were analyzed on 1% agarose gel and visualized under UV light after staining with ethidium bromide.
Sections of formalin-fixed, paraffin-embedded tumor samples (5 μm thick) were heated to 60°C and dehydrated in xylene and graded alcohols. Antigen retrieval was performed with 0.01 M citrate buffer at pH 6.0 for 20 minutes in a 95°C steam bath. Slides were allowed to cool for 20 minutes at room temperature, followed by repeated rinsing with 0.1 M phosphate-buffered saline (PBS, pH 7.4) containing 0.1% Tween 20 (PBS-T). Endogenous peroxidase activity was quenched with 3% hydrogen peroxidase. Each incubation step was conducted at room temperature and was followed by three sequential washes (5–10 minutes each) in PBS-T. Sections were incubated with anti-TG2 monoclonal antibodies, CUB-7401 (Neomarkers, Fremont, CA) overnight at 4°C, followed by incubation for 30 minutes each with biotinylated secondary antibody and peroxidase-labeled streptavidin. Antigen-antibody reactions were detected by exposure to 3,3'diaminobenzidine and hydrogen peroxide chromogen substrate (Vector Labs, Burlingame, CA) for 3–5 minutes. Slides were counterstained with hematoxylin and mounted. The negative controls were incubated with nonimmune mouse immunoglobulin g (IgG) in place of the primary antibody. The immunostained slides were examined under the light microscope and scored (with values of 0, 1+, 2+, or 3+) independently by two researchers in the laboratory.
Paraffin-embedded tissue sections from selected tumor samples were deparaffinized, washed 3 times with PBS, and blocked with 5% normal goat serum in PBS for 1 hour. The sections were immunostained by an indirect method using primary rabbit anti-TG2 (Neomarkers, Fremont, CA) and anti-isopeptide monoclonal Ab422 (Abcam, Cambridge, MA) antibodies. The anti-mouse IgG Alexa 488 and goat anti-rabbit IgG Alexa 546 (both from Molecular Probes, Eugene, OR) were used as the secondary antibodies. The immunostained sections were mounted in 80% glycerol and 20% PBS and viewed under the Zeiss Laser Scanning Microscope 510 (Carl Zeiss MicroImaging, Inc., Thornwood, NY) for taking the digital images. Appropriate controls, including mouse and rabbit IgG in place of the primary antibodies and either primary antibody alone along with both the secondary antibodies were included to determine the specificity of the reaction.
B-cell leukemia/lymphoma 2
epidermal growth factor receptor
focal adhesion kinase
transforming growth factor-beta.
The authors wish to thank Michael Gilogli and Jansina Y Fok for technical assistance and Mr. David Galloway for editorial help.
- Friedl P, Wolf K: Tumour-cell invasion and migration: diversity and escape mechanisms. Nature Rev Cancer. 2003, 3: 362-74. 10.1038/nrc1075.View ArticleGoogle Scholar
- Aznavoorian S, Murphy AN, Stetler-Stevenson WG, Liotta LA: Molecular aspects of tumor cell invasion and metastasis. Cancer. 1993, 71: 1368-83.View ArticlePubMedGoogle Scholar
- Stetler-Stevenson WG, Aznavoorian S, Liotta LA: Tumor cell interactions with the extracellular matrix during invasion and metastasis. Ann Rev Cell Biol. 1993, 9: 541-73.View ArticlePubMedGoogle Scholar
- Aeschlimann D, Thomazy V: Protein crosslinking in assembly and remodelling of extracellular matrices: the role of transglutaminases. Connect Tissue Res. 2000, 41: 1-27.View ArticlePubMedGoogle Scholar
- Fesus L, Piacentini M: Transglutaminase 2: an enigmatic enzyme with diverse functions. Trends Biochem Sci. 2002, 27: 534-9. 10.1016/S0968-0004(02)02182-5View ArticlePubMedGoogle Scholar
- Prince CW, Dickie D, Krumdieck CL: Osteopontin, a substrate for transglutaminase and factor XIII activity. Biochem Biophys Res Commun. 1991, 177: 1205-10. 10.1016/0006-291X(91)90669-XView ArticlePubMedGoogle Scholar
- Stephens P, Grenard P, Aeschlimann P, Langley M, Blain E, Errington R, Kipling D, Thomas D, Aeschlimann D: Crosslinking and G-protein functions of transglutaminase 2 contribute differentially fibroblast wound healing responses. Journal of Cell Sci. 2004, 117: 3389-3403. 10.1242/jcs.01188.View ArticleGoogle Scholar
- Chen JS, Mehta K: Tissue transglutaminase: an enzyme with a split personality. Int J Biochem Cell Biol. 1999, 31: 817-36. 10.1016/S1357-2725(99)00045-XView ArticlePubMedGoogle Scholar
- Lorand L, Graham RM: Transglutaminases: crosslinking enzymes with pleiotropic functions. Nature Rev Mol Cell Biol. 2003, 4: 140-56. 10.1038/nrm1014.View ArticleGoogle Scholar
- Aeschlimann D, Paulsson M: Cross-linking of laminin-nidogen complexes by tissue transglutaminase. A novel mechanism for basement membrane stabilization. J Biol Chem. 1991, 266: 15308-17.PubMedGoogle Scholar
- Kaartinen MT, Pirhonen A, Linnala-Kankkunen A, Maenpaa PH: Transglutaminase-catalyzed cross-linking of osteopontin is inhibited by osteocalcin. J Biol Chem. 1997, 272: 22736-41. 10.1074/jbc.272.36.22736View ArticlePubMedGoogle Scholar
- Kleman JP, Kleman JP, Aeschlimann D, Paulsson M, Vander Rest M: Transglutaminase-catalyzed cross-linking of fibrils of collagen V/XI in A204 rhabdomyosarcoma cells. Biochemistry. 1995, 34: 13768-75. 10.1021/bi00042a007View ArticlePubMedGoogle Scholar
- Griffin M, Smith LL, Wynne J: Changes in transglutaminase activity in an experimental model of pulmonary fibrosis induce by paraquat. Br J Exp Pathol. 1979, 60: 653-61.PubMed CentralPubMedGoogle Scholar
- Johnson TS, Griffin M, Thomas GL, Skill J, Cox A, Yang B, Nicholas B, Birckbichler PJ, Muchaneta-Kubara C, El Nahas AM: The role of transglutaminase in the rat subtotal nephrectomy model of renal fibrosis. J Clin Invest. 1997, 99: 2950-60.PubMed CentralView ArticlePubMedGoogle Scholar
- Gross SR, Balklava Z, Griffin M: Importance of tissue transglutaminase in repair of extracellular matrices and cell death of dermal fibroblasts after exposure to a solarium ultraviolet A source. J Invest Dermatol. 2003, 121: 412-23. 10.1046/j.1523-1747.2003.12353.xView ArticlePubMedGoogle Scholar
- Johnson TS, kill NJ, El Nahas AM, Oldroyd SD, Thomas GL, Douthwaite JA, Haylor JL, Griffin M: Transglutaminase transcription and antigen translocation in experimental renal scarring. J Am Soc Nephrol. 1999, 10: 2146-57.PubMedGoogle Scholar
- Nunes I, Gleizes PE, Metz CN, Rifkin DB: Latent transforming growth factor-beta binding protein domains involved in activation and transglutaminase-dependent cross-linking of latent transforming growth factor-beta. J Cell Biol. 1997, 136: 1151-63. 10.1083/jcb.136.5.1151PubMed CentralView ArticlePubMedGoogle Scholar
- Clark DA, Coker R: Transforming growth factor-beta (TGF-beta). Int J Biochem Cell Biol. 1998, 30: 293-8. 10.1016/S1357-2725(97)00128-3View ArticlePubMedGoogle Scholar
- Taipale J, Saharinen J, Keski-Oja J: Extracellular matrix-associated transforming growth factor-beta: role in cancer cell growth and invasion. Adv Cancer Res. 1998, 75: 87-134.View ArticlePubMedGoogle Scholar
- Stracke ML, Murata J, Aznavoorian S, Liotta LA: The role of the extracellular matrix in tumor cell metastasis. In Vivo. 1994, 8: 49-58.PubMedGoogle Scholar
- Wang RN, Zhu YB, Xue JY: The relation between integrin, type IV collagenase and extracellular matrix in invasion and metastasis of gastric carcinoma. Chinese J Pathol. 1994, 23: 278-81.Google Scholar
- Itano N, Yamada Y, Yoshida M, Kimata K: Cancer metastasis and extracellular matrix. Japn J Cancer Chemother. 1999, 26: 1663-8.Google Scholar
- Chen J, Kanopleva M, Multani A, Pathak S, Mehta K: Drug resistant breast cancer MCF-7 cells are paradoxically sensitive to apoptosis. J Cell Physiol. 2004, 200: 223-34. 10.1002/jcp.20014View ArticlePubMedGoogle Scholar
- Chen JS, Agarwal N, Mehta K: Multidrug-resistant MCF-7 breast cancer cells contain deficient intracellular calcium pools. Breast Cancer Res Treat. 2002, 71: 237-47. 10.1023/A:1014461832403View ArticlePubMedGoogle Scholar
- Devarajan E, Chen J, Multani AS, Pathak S, Sahin AA, Mehta K: Human breast cancer MCF-7 cell line contains inherently drug-resistant subclones with distinct genotypic and phenotypic features. Int J Oncol. 2002, 20: 913-20.PubMedGoogle Scholar
- Mehta K, Devarajan E, Chen J, Multani A, Pathak S: Multidrug-resistant MCF-7 cells: an identity crisis?. J Natl Cancer Inst. 2002, 94: 1652-4.View ArticlePubMedGoogle Scholar
- Mehta K: High levels of transglutaminase expression in doxorubicin-resistant human breast carcinoma cells. Int J Cancer. 1994, 58: 400-6.View ArticlePubMedGoogle Scholar
- Mangala LS, Mehta K: Tissue transglutaminase in cancer biology. Transglutaminases; the family of enzymes with diverse functions. Prog Exp Tumor Res. Edited by: Mehta K, Eckert R. 2005, 38: 125-138. Basel, Karger.Google Scholar
- Herman HF, Mehta K: Implications of increased tissue transglutaminase expression in drug-resistant breast cancer (MCF-7) cells. Mol Cancer Res. 2005, .Google Scholar
- Mehta K, Fok JY, Mangala SL: Tissue transglutaminase (TG2): from biological glue to signaling cues. Front Biosci. 2005, .Google Scholar
- Grigoriev MY, Suspitsin EN, Togo AV, Pozharisski KM, Ivanova OA, Nardacci R, Falasca L, Piacentini M, Imyanitov EN, Hanson KP: Tissue transglutaminase expression in breast carcinomas. J Exp Clin Cancer Res. 2001, 20: 265-8.PubMedGoogle Scholar
- Jiang WG, Ablin R, Douglas-Jones A, Mansel RE: Expression of transglutaminases in human breast cancer and their possible clinical significance. Oncol Rep. 2003, 10: 2039-44.PubMedGoogle Scholar
- Hettasch JM, Bandarenko N, Burchette JL, Lai TS, Marks JR, Haroon ZA, Peters K, Dewhirst MW, Iglehart JD, Greenberg CS: Tissue transglutaminase expression in human breast cancer. Lab Invest. 1996, 75: 637-45.PubMedGoogle Scholar
- Haroon ZA, Lai TS, Hettash JM, Lindberg RA, Dewhirst MW, Greenberg CS: Tissue transglutaminase is expressed as a host response to tumor invasion and inhibits tumor growth. Lab Invest. 1999, 79: 1679-86.PubMedGoogle Scholar
- Mapara MY, Sykes M: Tolerance and cancer: mechanisms of tumor evasion and strategies for breaking tolerance. J Clin Oncol. 2004, 22: 1136-51. 10.1200/JCO.2004.10.041View ArticlePubMedGoogle Scholar
- Lochter A, Sternlicht MD, Werb Z, Bissell MJ: The significance of matrix metalloproteinases during early stages of tumor progression. Ann NY Acad Sci. 1998, 857: 180-93.View ArticlePubMedGoogle Scholar
- Dano K, Romer J, Nielsen BS, Bjorn S, Pyke C, Rygaard J, Lund LR: Cancer invasion and tissue remodeling – cooperation of protease systems and cell types. Acta Pathol Immunol Microbiol Scand. 1999, 107: 120-7.View ArticleGoogle Scholar
- Werb Z, Vu TH, Rinkenberger JL, Coussens LM: Matrix-degrading proteases and angiogenesis during development and tumor formation. Acta Pathol Immunol Microbiol Scand. 1999, 107: 11-8.View ArticleGoogle Scholar
- Belkin AM, Zemskov EA, Hang J, Akimov SS, Sikora S, Strongin AY: Cell-surface-associated tissue transglutaminase is a target of MMP-2 proteolysis. Biochemistry. 2004, 43: 11760-69. 10.1021/bi049266zView ArticlePubMedGoogle Scholar
- Belkin AM, Akimov SS, Zaritskaya LS, Ratnikov BI, Deryugina EI, Strongin AY: Matrix-dependent proteolysis of surface transglutaminase by membrane-type metalloproteinase regulates cancer cell adhesion and locomotion. J Biol Chem. 2001, 276: 18415-22. 10.1074/jbc.M010135200View ArticlePubMedGoogle Scholar
- Koul D, Parathasarathy R, Shen R, Davies MA, Jasse SA, Chintala SK, Rao JS, Sun Y, Benvenisite EN, Liu TJ, Yung WKF: Suppression of metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN. Oncogene. 2001, 20: 6669-78. 10.1038/sj.onc.1204799View ArticlePubMedGoogle Scholar
- Mehta K, Fok J, Miller FR, Koul D, Sahin AA: Prognostic Significance of tissue transglutaminase in drug resistant and metastatic breast cancer. Clin Cancer Res. 2004, 10: 8068-8076.View ArticlePubMedGoogle Scholar
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