Chelate-soluble Pectin Fraction From Papaya Pulp Interacts With galectin-3 and Inhibits Colon Cancer Cell Proliferation
2019 (English)In: International Journal of Biological Macromolecules, ISSN 0141-8130, E-ISSN 1879-0003, Vol. 126, p. 170-178Article in journal (Refereed) Published
Abstract [en]
Colorectal cancer has an overexpression of galectin-3 that is related to cancer progression. A decreased risk of colon cancer can be related to consumption of dietary fibers, but the entire mechanism by which this protection occurs remains unclear. Pectin is a type of dietary fiber that possesses β-galactosides and can bind and inhibit galectin-3–mediated effects. Papaya fruit has a massive cell wall disassembling during ripening that naturally changes its pectin structure. Our work shows that different points in the ripening time of papaya fruit exhibit pectins (chelate-soluble fractions; CSF) that can or cannot inhibit galectin-3. The fraction that inhibits galectin-3 (3CSF) also diminishes the proliferation of colon cancer cell lines, and it is derived from an intermediate point of papaya ripening. Therefore, we related this to a papaya pectin structure-dependent effect, and the papaya fruit seems to have a pectin structure that is promising in decreasing the risk of colon cancer development.
Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 126, p. 170-178
Keywords [en]
Papaya pectin, Galectin-3, Colon cancer
National Category
Food Science
Identifiers
URN: urn:nbn:se:oru:diva-83476DOI: 10.1016/j.ijbiomac.2018.12.191ISI: 000460710000020PubMedID: 30584930Scopus ID: 2-s2.0-85059146023OAI: oai:DiVA.org:oru-83476DiVA, id: diva2:1445472
Note
Research supported by LNNano - Brazilian Nanotechnology National Laboratory, CNPEM/MCTI (Proposal AFM #21087). This research was financially supported by grants #2012/23970-2 and #2013/07914-8, São Paulo Research Foundation (FAPESP). Scholarships were awarded to SBRP by the National Council for Scientific and Technological Development (CNPq; 167934/2014-7).
2020-06-232020-06-232024-10-01Bibliographically approved