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Int J Biol Macromol. 2017 Oct;103:1000-1010. doi: 10.1016/j.ijbiomac.2017.05.137. Epub 2017 May 25.

The inhibitory effect of anti- tumor polysaccharide from Punica granatum on metastasis.

Author information

1
Laboratory of Biopharmaceuticals and Nanomedicine, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695011, Kerala, India. Electronic address: sheejava@gmail.com.
2
Laboratory of Biopharmaceuticals and Nanomedicine, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695011, Kerala, India. Electronic address: manumjoseph2000@gmail.com.
3
Laboratory of Biopharmaceuticals and Nanomedicine, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695011, Kerala, India. Electronic address: aravind_sr2003@yahoo.co.in.
4
Laboratory of Biopharmaceuticals and Nanomedicine, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695011, Kerala, India. Electronic address: ukbsbio@gmail.com.
5
Laboratory of Biopharmaceuticals and Nanomedicine, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695011, Kerala, India. Electronic address: ttsreelekha@gmail.com.

Abstract

Galactomannan (PSP001) isolated from the fruit rind of Punica granatum was demonstrated as an excellent antioxidant, immunomodulatory and anticancer agent both in vitro and in vivo models. Since the most lethal and debilitating attribute of cancer cells is their ability to evolve to a state of malignancy, with key features like increased angiogenesis, invasion, migration, colony formation, and metastasis, the present study focused on evaluating the effects of the galactomannan on tumor and malignancy. PSP001 effectively reduced the neovascularization in chick embryos highlighting its potential as an angiogenic inhibitor. Furthermore, the invasion, migration and clonogenic capacity of human and murine cancer cells were dramatically inhibited by PSP001. Evaluation of the molecular mechanism of its unique potential revealed the down regulation of key players including VEGF, MMP-2, and MMP-9 with marked elevation of TIMP-1 and TIMP-2. The anti-metastatic potential of PSP001 tested in pulmonary metastasis C57BL/6 mice model deciphered the combinatorial administration with vincristine deliberated better survival rates and decreased metastatic index. The angiogenic inhibition potential of PSP001 was further proved with peritoneal angiogenesis assay in BALB/c mice ascitic tumor model. The outcomes of the current investigation highlight the mode of action of antitumor galactomannan in the reduction of tumor malignancy.

KEYWORDS:

Punica granatum; anti-metastasis; neovascularization

PMID:
28552725
DOI:
10.1016/j.ijbiomac.2017.05.137
[Indexed for MEDLINE]

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