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Matrix Metalloproteinase-14 Expression and Its Prognostic Value in Cervical Carcinoma
Abstract
The objective of the study was to evaluate the expression of matrix metalloproteinase-14 (MMP-14) in cervical carcinoma and correlate its expression with clinicopathological parameters, recurrence, and survival of the patients. The expressions of MMP-14 in normal cervical mucosa and cervical carcinoma tissue were detected with immunohistochemistry. Survival analysis by the Kaplan-Meier method was performed to assess prognostic significance. The positive expression rate of MMP-14 in cervical carcinoma tissue was 81.6 %(111/136), and there was significant difference on their positive expression rates between in cervical carcinoma tissue and in normal cervical mucosa(22.4 %)(13/58)(P < 0.05);The positive expression rates of MMP-14 in patients with poor histologic differentiation, lymph node metastasis, and recurrence group were heightened. Using Kaplan-Meier analysis, a comparison of survival curves of low versus high expressions of MMP-14 revealed a highly significant difference in human cervical carcinoma tissue (P < 0.05), which suggests that overexpression of MMP-14 is associated with a worse prognosis. The MMP-14 which promotes angiogenes is associated with lymph node metastasis, vascular invasion, and poor prognosis of cervical carcinoma. The current study shows that MMP-14 may be an independent prognostic factor for cervical carcinoma patients.
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“the upregulation of MMP1, MT1-MMP, MMP2 and MMP9 has been shown to be due to the expression of HPV E6 and E7 oncoproteins in various cellular models of cervical cancer [260,261,262,263,264]”
From The Not-So-Good, the Bad and the Ugly: HPV E5, E6 and E7 Oncoproteins in the Orchestration of Carcinogenesis (2021) · cites this paper as [261]
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- Devy, L., Huang, L., Naa, L., Yanamandra, N., Pieters, H., et al. (2009). Selective inhibition of matrix metalloproteinase-14 blocks tumor growth, invasion, and angiogenesis. Cancer Research, 69, 1517–1526. · DOI
- Kim, G. E., Kim, J. H., Lee, K. H., Choi, Y. D., Lee, J. S., et al. (2012). Stromal matrix metalloproteinase-14 expression correlates with the grade and biological behavior of mammary phyllodes tumors. Applied Immunohistochemistry & Molecular Morphology, 20, 298–303. · DOI
- Zhang, H., Qi, M., Li, S., Qi, T., Mei, H., et al. (2012). microRNA-9 targets matrix metalloproteinase 14 to inhibit invasion, metastasis, and angiogenesis of neuroblastoma cells. Molecular Cancer Therapeutics, 11, 1454–1466. · DOI
- Watanabe, H. (2010). Extracellular matrix–regulation of cancer invasion and metastasis. Gan To Kagaku Ryoho, 37, 2058–2061.
- Tee, Y. T., Han, C. P., Ko, J. L., Chen, G. D., Yang, S. F., et al. (2007). Evaluation of matrix metalloproteinase 2 expression in cervical carcinogenesis using tissue array and integrated optical density for immunoreactivity. Reproductive Sciences, 14, 719–726. · DOI
- Zarrabi, K., Dufour, A., Li, J., Kuscu, C., Pulkoski-Gross, A., et al. (2011). Inhibition of matrix metalloproteinase 14 (MMP-14) -mediated cancer cell migration. Journal of Biological Chemistry, 286, 33167–33177. · DOI · Paper page
- Chen, T. Y., Li, Y. C., Liu, Y. F., Tsai, C. M., Hsieh, Y. H., et al. (2011). Role of MMP14 gene polymorphisms in susceptibility and pathological development to hepatocellular carcinoma. Annals of Surgical Oncology, 18, 2348–2356. · DOI
- Dong, Q., Yu, D., Yang, C. M., Jiang, B., & Zhang, H. (2010). Expression of the reversion-inducing cysteine-rich protein with Kazal motifs and matrix metalloproteinase-14 in neuroblastoma and the role in tumour metastasis. International Journal of Experimental Pathology, 91, 368–373. · DOI
- Laudański, P., Swiatecka, J., Kozłowski, L., Leśniewska, M., Wojtukiewicz, M., et al. (2010). Increased serum level of membrane type 1-matrix metalloproteinase (MT1-MMP/MMP-14) in patients with breast cancer. Folia Histochemica et Cytobiologica, 48, 101–103. · DOI
- Littlepage, L. E., Sternlicht, M. D., Rougier, N., Phillips, J., Gallo, E., et al. (2010). Matrix metalloproteinases contribute distinct roles in neuroendocrine prostate carcinogenesis, metastasis, and angiogenesis progression. Cancer Research, 70, 2224–2234. · DOI
- Fidler, I. J. (2000). Angiogenesis and cancer metastasis. Cancer Journal, 2, S134–S141.
- Cork, S. M., Kaur, B., Devi, N. S., Cooper, L., Saltz, J., et al. (2012). A proprotein convertase/MMP-14 proteolytic cascade releases a novel 40 kDa vasculostatin from tumor suppressor BAI1. Oncogene, 31(50), 5144–5152. · DOI
- Aplin, A. C., Zhu, W. H., Fogel, E., & Nicosia, R. F. (2009). Vascular regression and survival are differentially regulated by MT1-MMP and TIMPs in the aortic ring model of angiogenesis. American Journal of Physiology. Cell Physiology, 297, C471–C480. · DOI
- Devy, L., Huang, L., Naa, L., Yanamandra, N., Pieters, H., et al. (2009). Selective inhibition of matrix metalloproteinase-14 blocks tumor growth, invasion, and angiogenesis. Cancer Research, 69, 1517–1526. · DOI
- Roebuck, M. M., Helliwell, T. R., Chaudhry, I. H., Kalogrianitis, S., Carter, S., et al. (2005). Matrix metalloproteinase expression is related to angiogenesis and histologic grade in spindle cell soft tissue neoplasms of the extremities. American Journal of Clinical Pathology, 123, 405–414. · DOI
- Ricke, W. A., Smith, G. W., Reynolds, L. P., Redmer, D. A., & Smith, M. F. (2002). Matrix metalloproteinase (2, 9, and 14) expression, localization, and activity in ovine corpora lutea throughout the estrous cycle. Biology of Reproduction, 66, 1083–1094. · DOI
- Niewiarowska, J., Brézillon, S., Sacewicz-Hofman, I., Bednarek, R., Maquart, F. X., et al. (2011). Lumican inhibits angiogenesis by interfering with α2β1 receptor activity and downregulating MMP-14 expression. Thrombosis Research, 128, 452–457. · DOI
- Heikkilä, P., Teronen, O., Hirn, M. Y., Sorsa, T., Tervahartiala, T., et al. (2003). Inhibition of matrix metalloproteinase-14 in osteosarcoma cells by clodronate. Journal of Surgical Research, 111, 45–52. · DOI
- Naglich, J. G., Jure-Kunkel, M., Gupta, E., Fargnoli, J., Henderson, A. J., et al. (2001). Inhibition of angiogenesis and metastasis in two murine models by the matrix metalloproteinase inhibitor, BMS-275291. Cancer Research, 61, 8480–8485.
- Zhai, Y., Hotary, K. B., Nan, B., Bosch, F. X., Muñoz, N., et al. (2005). Expression of membrane type 1 matrix metalloproteinase is associated with cervical carcinoma progression and invasion. Cancer Research, 65, 6543–6550. · DOI · Paper page
- Shields, M. A., Dangi-Garimella, S., Redig, A. J., & Munshi, H. G. (2012). Biochemical role of the collagen-rich tumour microenvironment in pancreatic cancer progression. Biochemical Journal, 441, 541–552. · DOI
- Poincloux, R., Lizárraga, F., & Chavrier, P. (2009). Matrix invasion by tumour cells: A focus on MT1-MMP trafficking to invadopodia. Journal of Cell Science, 122, 3015–3024. · DOI
- Wolf, K., Wu, Y. I., Liu, Y., Geiger, J., Tam, E., et al. (2007). Multi-step pericellular proteolysis controls the transition from individual to collective cancer cell invasion. Nature Cell Biology, 9, 893–904. · DOI
- von Lampe, B., Barthel, B., Coupland, S. E., Riecken, E. O., & Rosewicz, S. (2000). Differential expression of matrix metalloproteinases and their tissue inhibitors in colon mucosa of patients with inflammatory bowel disease. Gut, 47, 63–73. · DOI
- Kim, J. H., Kim, T. H., Jang, J. W., Jang, Y. J., Lee, K. H., et al. (2001). Analysis of matrix metalloproteinase mRNAs expressed in hepatocellular carcinoma cell lines. Molecules and Cells, 12, 32–40. · DOI
Cited by
Basukala, O., & Banks, L. (2021) · Viruses · doi:10.3390/v13101892 · Cited by 137
Metadata
- Authors
- Wang, H., Zhang, X., Huang, L., Li, J., Qu, S., & Pan, F.
- Venue
- Cell Biochemistry and Biophysics
- Published
- 2014-05-01
- Volume
- 70
- Issue
- 2
- Pages
- 729-734
- ISSN
- 1085-9195
- 1559-0283
- Cited by
- 16
- References
- 0
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
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