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Momordica cochinchinensis Seed Extracts Suppress Migration and Invasion of Human Breast Cancer ZR-75-30 Cells Via Down-regulating MMP-2 and MMP-9

  • Published : 2014.02.01

Abstract

Objective: Metastases and invasion are the main reasons for oncotherapy failure. Momordica cochinchinensis (Mu Bie Zi in Chinese) had been used for a variety of purposes, and shown anti-cancer action. In this article, we focused on effects on regulation of breast cancer cell ZR-75-30 metastases and invasion by extracts of Momordica cochinchinensis seeds (ESMCs). Methods: Effect of ESMCs on ZR-75-30 human breast cancer cells proliferation were evaluated by MTT assay and on invasion and migration by wound-healing and matrigel invasion chamber assays. Expression and protease activity of two matrix metalloproteinases (MMPs), MMP-2 and MMP-9, were analyzed by Western blotting and gelatin zymography, respectively. Results: ESMC revealed strong growth inhibitory effects on ZR-75-30 cells, and effectively inhibited ZR-75-30 cell invasion in a dose-dependent manner. Western blot and gelatin zymography analysis showed that ESMC significantly inhibited the expression and secretion of MMP-2 and MMP-9 in ZR-75-30 cells. Conclusions: ESMC has the potential to suppress the migration and invasion of ZR-75-30 cancer cells, and it might prove to of interest in the development of novel inhibitors for breast cancer.

Keywords

References

  1. Chambers AF, Groom AC, MacDonald IC (2002). Dissemination and growth of cancer cells in metastatic sites. Nat Rev Cancer, 2, 563-72. https://doi.org/10.1038/nrc865
  2. Fang Y, Chen Y, Yu L, et al (2013). Inhibition of breast cancer metastases by a novel inhibitor of TGFbeta receptor 1. J Natl Cancer Inst, 105, 47-58. https://doi.org/10.1093/jnci/djs485
  3. Friedl P, Wolf K (2003). Tumour-cell invasion and migration: diversity and escape mechanisms. Nat Rev Cancer, 3, 362-74. https://doi.org/10.1038/nrc1075
  4. Gordon M. Cragg, Newman DJ (2005). Plants as a source of anti-cancer agents. J Ethnopharmacol, 100, 72-9. https://doi.org/10.1016/j.jep.2005.05.011
  5. Hidalgo M, Eckhardt SG (2001). Development of matrix metalloproteinase inhibitors in cancer therapy. J Natl Cancer Inst, 93, 178-93. https://doi.org/10.1093/jnci/93.3.178
  6. Ishida BK, Turner C, Chapman MH, Mckeon TA (2004). Fatty acid and carotenoid composition of gac (Momordica cochinchinensis Spreng) fruit. J Agr Food Chem, 52, 274-79. https://doi.org/10.1021/jf030616i
  7. Kubola J, Siriamornpun S (2011). Phytochemicals and antioxidant activity of different fruit fractions (peel, pulp, aril and seed) of Thai gac (Momordica cochinchinensis Spreng). Food Chem, 127, 1138-45. https://doi.org/10.1016/j.foodchem.2011.01.115
  8. Lin ZY, Liu X, Yang F, Yu YQ (2012). Structural characterization and identification of five triterpenoid saponins isolated from Momordica cochinchinensis extracts by liquid chromatography/tandem mass spectrometry. Int J Mass Spectrom, 328-329, 43-66. https://doi.org/10.1016/j.ijms.2012.07.022
  9. Mendes O, Kim HT, Stoica G (2005). Expression of MMP2, MMP9 and MMP3 in breast cancer brain metastasis in a rat model. Clin Exp Metastas, 22, 237-46. https://doi.org/10.1007/s10585-005-8115-6
  10. Mueller A, Homey B, Soto H, et al (2001). Involvement of chemokine receptors in breast cancer. Nature, 410, 50-6. https://doi.org/10.1038/35065016
  11. Munkhzaya B., Joseph C., Seung HY, Seong H (2013). Anti-metastatic potential of ethanol extract of Saussurea involucrata against hepatic cancer in vitro. Asian Pac J Cancer P, 14, 5397-402. https://doi.org/10.7314/APJCP.2013.14.9.5397
  12. Parks SE, Murray CT, Gale DL, et al (2012). Propagation and production of Gac (Momordica Cochinchinensis Spreng.), a Greenhouse Case Study. Exp Agr, 49, 234-43.
  13. Rooprai H, Rucklidge G, Panou C, Pilkington G (2000). The effects of exogenous growth factors on matrix metalloproteinase secretion by human brain tumour cells. Brit J Cancer, 82, 52-5. https://doi.org/10.1054/bjoc.1999.0876
  14. Sanwal SK, Singh B, Kozak M, et al (2011). Yield improvement through female homosexual hybrids and sex genetics of sweet gourd (Momordica cochinchinensis Spreng.) ACTA Physiol Plant, 33, 1991-6. https://doi.org/10.1007/s11738-010-0693-5
  15. Somiari SB, Somiari RI, Heckman CM, et al (2006). Circulating MMP2 and MMP9 in breast cancer - potential role in classification of patients into low risk, high risk, benign disease and breast cancer categories. Int J Cancer, 119, 1403-11. https://doi.org/10.1002/ijc.21989
  16. Song FQ, Liu Y, Kong XS, Chang W, Song G (2013). Progress on understanding the anticancer mechanisms of medicinal mushroom: Inonotus Obliquus. Asian Pac J Cancer P, 14, 1571-8. https://doi.org/10.7314/APJCP.2013.14.3.1571
  17. Tsoi AYK, Ng TB, Fong WP (2006). Immunomodulatory activity of a chymotrypsin inhibitor from Momordica cochinchinensis seeds. J Pept Sci, 12, 605-11. https://doi.org/10.1002/psc.765
  18. Waraporn Y, Athikom S, Roongtawan S (2013). Suppression of human fibrosarcoma cell metastasis by Phyllanthus emblica extract in vitro. Asian Pac J Cancer Prev, 14, 6863-7. https://doi.org/10.7314/APJCP.2013.14.11.6863
  19. Weigelt B, Peterse JL, van 't Veer LJ (2005). Breast cancer metastasis: markers and models. Nat Rev Cancer, 5, 591-602. https://doi.org/10.1038/nrc1670
  20. Wong RCH, Fong WP, Ng TB (2004). Multiple trypsin inhibitors from Momordica cochinchinensis seeds, the Chinese drug mubiezhi. Peptides, 25, 163-9. https://doi.org/10.1016/j.peptides.2004.01.002
  21. Yilmaz M, Christofori G. Lehembre F (2007). Distinct mechanisms of tumor invasion and metastasis. Trends Mol Med, 13, 535-41. https://doi.org/10.1016/j.molmed.2007.10.004
  22. Zheng L, Wang XL, Luo WJ, et al (2013). Brucine, an effective natural compound derived from nux-vomica, induces G1 phase arrest and apoptosis in LoVo cells. Food Chem Toxicol, 58, 332-9. https://doi.org/10.1016/j.fct.2013.05.011

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