α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells

  • Authors:
    • Xiang Fan
    • Lingli He
    • Yao Meng
    • Gangrui Li
    • Linli Li
    • Yanfa Meng
  • View Affiliations

  • Published online on: January 9, 2015     https://doi.org/10.3892/mmr.2015.3176
  • Pages: 3553-3558
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Abstract

α‑Momorcharin (α‑MMC) and momordica anti‑human immunodeficiency virus protein (MAP30), produced by Momordica charantia, are ribosome‑inactivating proteins, which have been reported to exert inhibitory effects on cultured tumor cells. In order to further elucidate the functions of these agents, the present study aimed to investigate the effects of α‑MMC and MAP30 on cell viability, the induction of apoptosis, cell cycle arrest, DNA integrity and superoxide dismutase (SOD) activity. α‑MMC and MAP30 were purified from bitter melon seeds using ammonium sulfate precipitation in combination with sulfopropyl (SP)‑sepharose fast flow, sephacryl S‑100 and macro‑Cap‑SP chromatography. MTT, flow cytometric and DNA fragmentation analyses were then used to determine the effects of α‑MMC and MAP30 on human lung adenocarcinoma epithelial A549 cells. The results revealed that A549 cells were sensitive to α‑MMC and MAP30 cytotoxicity assays in vitro. Cell proliferation was significantly suppressed following α‑MMC and MAP30 treatment in a dose‑ and time‑dependent manner; in addition, the results indicated that MAP30 had a more potent anti‑tumor activity compared with that of α‑MMC. Cell cycle arrest in S phase and a significantly increased apoptotic rate were observed following treatment with α‑MMC and MAP30. Furthermore, DNA integrity analysis revealed that the DNA of A549 cells was degraded following treatment with α‑MMC and MAP30 for 48 h. The pyrogallol autoxidation method and nitrotetrazolium blue chloride staining were used to determine SOD activity, the results of which indicated that α‑MMC and MAP30 did not possess SOD activity. In conclusion, the results of the present study indicated that α‑MMC and MAP30 may have potential as novel therapeutic agents for the prophylaxis and treatment of cancer.

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May-2015
Volume 11 Issue 5

Print ISSN: 1791-2997
Online ISSN:1791-3004

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Spandidos Publications style
Fan X, He L, Meng Y, Li G, Li L and Meng Y: α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells. Mol Med Rep 11: 3553-3558, 2015.
APA
Fan, X., He, L., Meng, Y., Li, G., Li, L., & Meng, Y. (2015). α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells. Molecular Medicine Reports, 11, 3553-3558. https://doi.org/10.3892/mmr.2015.3176
MLA
Fan, X., He, L., Meng, Y., Li, G., Li, L., Meng, Y."α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells". Molecular Medicine Reports 11.5 (2015): 3553-3558.
Chicago
Fan, X., He, L., Meng, Y., Li, G., Li, L., Meng, Y."α‑MMC and MAP30, two ribosome‑inactivating proteins extracted from Momordica charantia, induce cell cycle arrest and apoptosis in A549 human lung carcinoma cells". Molecular Medicine Reports 11, no. 5 (2015): 3553-3558. https://doi.org/10.3892/mmr.2015.3176