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Migration and proliferation of cancer cells in culture are differentially affected by molecular size of modified citrus pectin
Department of Food Science and Experimental Nutrition, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, SP, Brazil.ORCID-id: 0000-0003-4627-6291
Department of Food Science and Experimental Nutrition, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Departments of Oncology and Pathology, School of Medicine, Wayne State University, Detroit, MI, USA; Karmanos Cancer Institute, Detroit, MI, USA; Department of Maxillofacial Surgery, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Departments of Oncology and Pathology, School of Medicine, Wayne State University, Detroit, MI, USA; Karmanos Cancer Institute, Detroit, MI, USA.
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2019 (engelsk)Inngår i: Carbohydrate Polymers, ISSN 0144-8617, E-ISSN 1879-1344, Vol. 211, s. 141-151Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

While chemically and thermally modified citrus pectin (MCP) has already been studied for health benefits, it is unknown how size-fractionated oligo- and polysaccharides differentially affect cancer cell behavior. We produced thermally MCP and fractionated it by molecular size to evaluate the effect these polymers have on cancer cells. MCP30/10 (between 30 and 10 kDa) had more esterified homogalacturonans (HG) and fewer rhamnogalacturonans (RG-I) than MCP and MCP30 (higher than 30 kDa), while MCP10/3 (between 10 and 3 kDa) showed higher amounts of type I arabinogalactans (AGI) and lower amounts of RG-I. MCP3 (smaller than 3 kDa) presented less esterified HG and the lowest amount of AGI and RG-I. Our data indicate that the enrichment of de-esterified HG oligomers and the AGI and RG-I depletions in MCP3, or the increase of AGI and loss of RGI in MCP30/10, enhance the anticancer behaviors by inhibiting migration, aggregation, and proliferation of cancer cells.

sted, utgiver, år, opplag, sider
Elsevier, 2019. Vol. 211, s. 141-151
Emneord [en]
Pectin, Modified pectin, Citrus, Cancer cells
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Identifikatorer
URN: urn:nbn:se:oru:diva-83473DOI: 10.1016/j.carbpol.2019.02.010ISI: 000459866600017PubMedID: 30824074Scopus ID: 2-s2.0-85061083266OAI: oai:DiVA.org:oru-83473DiVA, id: diva2:1445460
Merknad

This research was financially supported by grants #2012/23970-2 and #2013/07914-8, São Paulo Research Foundation (FAPESP). A multiuser equipment was used (#2015/01004-5, São Paulo Research Foundation (FAPESP)). Scholarships were awarded to SBRP by the National Council for Scientific and Technological Development (CNPq; 167934/2014-7) and to TMS (CAPES Process BEX-10734/13-9).

Tilgjengelig fra: 2020-06-23 Laget: 2020-06-23 Sist oppdatert: 2024-11-11bibliografisk kontrollert

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