﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>BioImpacts</JournalTitle>
      <Issn>2228-5652</Issn>
      <Volume>11</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2021</Year>
        <Month>07</Month>
        <DAY>30</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Cell cycle arrest and anti-cancer potential of probiotic Lactobacillus rhamnosus against HT-29 cancer cells</ArticleTitle>
    <FirstPage>245</FirstPage>
    <LastPage>252</LastPage>
    <ELocationID EIdType="doi">10.34172/bi.2021.32</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Najme</FirstName>
        <LastName>Dehghani</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-5340-4963</Identifier>
      </Author>
      <Author>
        <FirstName>Farzaneh</FirstName>
        <LastName>Tafvizi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-3595-5021</Identifier>
      </Author>
      <Author>
        <FirstName>Parvaneh</FirstName>
        <LastName>Jafari</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/bi.2021.32</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>04</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>04</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Nowadays, probiotic bacteria have been considered as a factor in the prevention and treatment of cancer, especially by induction of apoptosis. This study aimed to evaluate the cytotoxic, anti-proliferative, and apoptotic effects of the supernatant of probiotic Lactobacillus rhamnosus on HT-29 cell line. Methods: Molecular identification of probiotic L. rhamnosus was carried out using specific primers of 16S rRNA gene and sequencing. HT-29 cells were treated with different concentrations of bacterial supernatants at 24, 48, and 72 hours. MTT assay, Annexin V-FITC, real-time PCR, cell cycle analysis, and DAPI staining tests were conducted to evaluate the induction of apoptosis. The level of cyclin D1 protein was measured by immunocytochemistry method. Results: The supernatant of L. rhamnosus inhibited the growth of HT-29 cancer cells in a dose- and time-dependent manner. The results of flow cytometry confirmed apoptotic cell death. Probiotic bacterial supernatant caused up-regulation of pro-apoptotic genes including caspase-3, caspase-9, and Bax. In addition, they resulted in down-regulation of Bcl2 and a decrease in expression levels of cyclin D1, cyclin E, and ERBB2 genes. Cancer cells were arrested in the G0/G1 phase of the cell cycle. The results of immunocytochemistry showed significant down-regulation of cyclin D1 protein during the 48 hours treatment with bacterial supernatant compared to the untreated cells. Conclusion: The supernatant of probiotic L. rhamnosus has a great potential to inhibit the proliferation of HT-29 cells and the induction of apoptosis. L. rhamnosus might be used as a biological anti-cancer factor in the prevention and treatment of colon cancer.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Apoptosis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Colon cancer</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Lactobacillus rhamnosus</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Probiotic</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Supernatant</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>