ЕКСТРАКТ ІЗ ВИСІВОК ЧЕРВОНОГО РИСУ ПРИГНІЧУЄ ПРОЛІФЕРАЦІЮ КЛІТИН РАКУ ТОВСТОЇ КИШКИ ШЛЯХОМ ІНДУКЦІЇ АПОПТОЗУ І ЗУПИНКИ КЛІТИННОГО ЦИКЛУ ТА ПРОЯВЛЯЄ АНТИМУТАГЕННУ АКТИВНІСТЬ

Background. Red rice bran extract (RRBE) contains many biologically active substances exerting antioxidant and anti-inflammatory effects. Aim. To evaluate the anticancer potential of RRBE in human colon cancer cells and its mutagenic/antimutagenic effects on nonmalignant cells. Materials and Methods...

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Bibliographic Details
Date:2023
Main Authors: Praphasawat, Ratsada, Palipoch, Sarawoot, Suwannalert, Prasit, Payuhakrit, Witchuda, Kunsorn, Paween, Laovitthayanggoon, Sarunya, Thakaew, Sinittra, Munkong, Narongsuk, Klajing, Warangkhana
Format: Article
Language:Ukrainian
Published: PH Akademperiodyka 2023
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Online Access:https://exp-oncology.com.ua/index.php/Exp/article/view/2023-2-10
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Journal Title:Experimental Oncology

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Experimental Oncology
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Summary:Background. Red rice bran extract (RRBE) contains many biologically active substances exerting antioxidant and anti-inflammatory effects. Aim. To evaluate the anticancer potential of RRBE in human colon cancer cells and its mutagenic/antimutagenic effects on nonmalignant cells. Materials and Methods. The cytotoxic effect of RRBE was determined by trypan blue exclusion in HCT116, HT29 cell lines and a non-cancerous HEK293 cell line, and its antiproliferative effect using MTS and colony formation assay. The apoptosis induction was evaluated using ELISA, and the apoptotic rate and cell cycle progression were assessed by flow cytometry. The mutagenic/ antimutagenic potential of RRBE was analyzed by micronucleus assay in the V79 cell line. Results. RRBE caused a dose-dependent reduction of cell viability in colon cancer cells and showed a limited cytotoxicity against HEK293 cells. The treatment with RRBE suppressed proliferation of HCT116 and HT29 cells and induced apoptosis as evidenced by the increased DNA fragmentation and the apoptotic cell counts. Furthermore, RRBE treatment significantly increased the number of cells at the G2/M phase triggering the arrest of the cell cycle in colon cancer cells. Interestingly, RRBE did not increase the micronucleus frequency in V79 cells but reduced the micronucleus formation caused by mitomycin C. Conclusion. RRBE effectively suppressed proliferation, induced apoptosis, and caused a cell cycle arrest in human colon cancer cells while being non-mutagenic and exerting antimutagenic effects in vitro.