Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colonsVisa övriga samt affilieringar
2024 (Engelska)Ingår i: Carbohydrate Polymers, ISSN 0144-8617, E-ISSN 1879-1344, Vol. 331, artikel-id 121878Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Pectins are a class of soluble polysaccharides that can have anticancer properties through several mechanisms. This study aimed to characterize the molecular structure of water-soluble fractions (WSF) derived from ripe and unripe papayas and assess their biological effects in two models: the 3D colon cancer spheroids to measure cell viability and cytotoxicity, and the in vivo model to investigate the inhibition of preneoplastic lesions in rats. WSF yield was slightly higher in ripe papaya, and both samples mainly consisted of pectin. Both pectins inhibited the growth of colon cancer HT29 and HCT116 spheroids. Unripe pectin disturbed HT29/NIH3T3 spheroid formation, decreased HCT116 spheroid viability, and increased spheroid cytotoxicity. Ripe pectin had a more substantial effect on the reduction of spheroid viability for HT29 spheroids. Furthermore, in vivo experiments on a rat model revealed a decrease in aberrant crypt foci (ACF) formation for both pectins and increased apoptosis in colonocytes for ripe papaya pectins. The results suggest potential anticancer properties of papaya pectin, with ripe pectin showing a higher potency.
Ort, förlag, år, upplaga, sidor
Elsevier, 2024. Vol. 331, artikel-id 121878
Nyckelord [en]
Pectin, Anticancer, Spheroids, Wistar rat, Aberrant crypt foci, Papaya
Nationell ämneskategori
Cancer och onkologi Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)
Identifikatorer
URN: urn:nbn:se:oru:diva-112830DOI: 10.1016/j.carbpol.2024.121878ISI: 001180827900001PubMedID: 38388061Scopus ID: 2-s2.0-85184008768OAI: oai:DiVA.org:oru-112830DiVA, id: diva2:1848697
Anmärkning
This work was supported by the São Paulo Research Foundation (FAPESP) for J.L.S.D. scholarships (2019/018794-0 and 2021/07292-3); The National Council for Scientific and Technological Development (CNPq) for J.P.F. productivity scholarship (CNPq Proc. #307842/2022-3); the São Paulo Research Foundation (FAPESP) financially supported by grants #2013/07914-8 and #2022/12834-2.
2024-04-042024-04-042025-01-20Bibliografiskt granskad