Role of exosomal miRNA in chemotherapy resistance of Colorectal cancer: A systematic review

The third most common malignancy has been identified as Colorectal cancer (CRC) that conducive to death in most cases. Chemoresistance is a common obstacle to CRC treatment. Circulating exosomal microRNAs (miRNAs) have been shown to reverse chemo‐resistance and are promising biomarkers for CRC. The...

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Veröffentlicht in:Chemical biology & drug design 2023-05, Vol.101 (5), p.1096-1112
Hauptverfasser: Maleki, Masomeh, Golchin, Asal, Javadi, Samira, Khelghati, Nafiseh, Morovat, Pejman, Asemi, Zatollah, Alemi, Forough, Vaghari‐Tabari, Mostafa, Yousefi, Bahman, Majidinia, Maryam
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container_issue 5
container_start_page 1096
container_title Chemical biology & drug design
container_volume 101
creator Maleki, Masomeh
Golchin, Asal
Javadi, Samira
Khelghati, Nafiseh
Morovat, Pejman
Asemi, Zatollah
Alemi, Forough
Vaghari‐Tabari, Mostafa
Yousefi, Bahman
Majidinia, Maryam
description The third most common malignancy has been identified as Colorectal cancer (CRC) that conducive to death in most cases. Chemoresistance is a common obstacle to CRC treatment. Circulating exosomal microRNAs (miRNAs) have been shown to reverse chemo‐resistance and are promising biomarkers for CRC. The capacity of engineered exosomes to cross biological barriers and deliver functional miRNAs could be used to achieve these proposes. The object of this review is the investigation of the role of exosomal miRNA in the chemo‐resistance, diagnosis, and prognosis of CRC. Using Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guidelines, electronic databases, PubMed, EMBASE, Web of Science, Scopus were searched from January 1990 to November 2020. Ultimately, eight articles included five in vitro (16 cell lines) and three in vivo examinations. Three studies demonstrated that increasing or decreasing mRNA expression was associated with increasing and decreasing cell proliferation in vitro. The presence of miRNA in two studies increased the sensitivity of the drug and exhibited a considerable growth inhibitory effect on cancer cell proliferation. The apoptotic rate was significantly increased in four studies by increased mRNA expression and reduced mrna expression. Tumor volume of xenograft models in three studies suppressed by antitumor miRNA activity. In contrast, anti‐miRNA activity in one study decreased the tumor volume. Exosomal miRNAs can be regulators of chemo‐resistance and predict adverse outcomes in CRC patients. In sum, exosomes containing miRNAs can be a promising biomarker for the prognosis and diagnosis of CRC. Subsequent research should be a focus on delineating the function of exosomal miRNA before clinical use. Exosomes are used as a biological transfer medium for targeted tumor therapy due to their high capacity to cross biological barriers and functionally deliver the miRNAs. Targeted delivery of engineered miRNA‐containing exosomes can reverse the chemotherapy drug resistance, and are promising biomarkers for the diagnosis and prognosis of colorectal cancer.
doi_str_mv 10.1111/cbdd.13947
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Chemoresistance is a common obstacle to CRC treatment. Circulating exosomal microRNAs (miRNAs) have been shown to reverse chemo‐resistance and are promising biomarkers for CRC. The capacity of engineered exosomes to cross biological barriers and deliver functional miRNAs could be used to achieve these proposes. The object of this review is the investigation of the role of exosomal miRNA in the chemo‐resistance, diagnosis, and prognosis of CRC. Using Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guidelines, electronic databases, PubMed, EMBASE, Web of Science, Scopus were searched from January 1990 to November 2020. Ultimately, eight articles included five in vitro (16 cell lines) and three in vivo examinations. Three studies demonstrated that increasing or decreasing mRNA expression was associated with increasing and decreasing cell proliferation in vitro. The presence of miRNA in two studies increased the sensitivity of the drug and exhibited a considerable growth inhibitory effect on cancer cell proliferation. The apoptotic rate was significantly increased in four studies by increased mRNA expression and reduced mrna expression. Tumor volume of xenograft models in three studies suppressed by antitumor miRNA activity. In contrast, anti‐miRNA activity in one study decreased the tumor volume. Exosomal miRNAs can be regulators of chemo‐resistance and predict adverse outcomes in CRC patients. In sum, exosomes containing miRNAs can be a promising biomarker for the prognosis and diagnosis of CRC. Subsequent research should be a focus on delineating the function of exosomal miRNA before clinical use. Exosomes are used as a biological transfer medium for targeted tumor therapy due to their high capacity to cross biological barriers and functionally deliver the miRNAs. 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Targeted delivery of engineered miRNA‐containing exosomes can reverse the chemotherapy drug resistance, and are promising biomarkers for the diagnosis and prognosis of colorectal cancer.</description><subject>Biomarkers, Tumor - metabolism</subject><subject>chemotherapy</subject><subject>colorectal cancer</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - genetics</subject><subject>exosome</subject><subject>Exosomes - genetics</subject><subject>Exosomes - metabolism</subject><subject>Exosomes - pathology</subject><subject>Humans</subject><subject>microRNAs</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>RNA, Messenger - metabolism</subject><issn>1747-0277</issn><issn>1747-0285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90E1LwzAcx_EgipvTiy9AehShM09tUm-z8wmGwtCTh5Il_7JIu8ykc_bd2226o7kkhA-_wxehc4KHpDvXembMkLCMiwPUJ4KLGFOZHO7fQvTQSQgfGHOeUHmMeoxziRNC-uh96iqIXBnBtwuuVlVU2-nzKLKLSM-hds0cvFq2kYdgQ6MWeotzVzkPuum43vz5m2gUhTY0UKvG6k5_WVifoqNSVQHOfu8Beru_e80f48nLw1M-msSa0UzEDJMso0KCxoJIwCU2jCSSAzEq5Vgbg1PKEs1kmZaCpDKjKs1SIyhLSZJQNkCXu92ld58rCE1R26ChqtQC3CoUNEkzJnhXqKNXO6q9C8FDWSy9rZVvC4KLTcxiE7PYxuzwxe_ualaD2dO_eh0gO7C2FbT_TBX57Xi8G_0BI4t9YA</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Maleki, Masomeh</creator><creator>Golchin, Asal</creator><creator>Javadi, Samira</creator><creator>Khelghati, Nafiseh</creator><creator>Morovat, Pejman</creator><creator>Asemi, Zatollah</creator><creator>Alemi, Forough</creator><creator>Vaghari‐Tabari, Mostafa</creator><creator>Yousefi, Bahman</creator><creator>Majidinia, Maryam</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9776-5816</orcidid><orcidid>https://orcid.org/0000-0002-4220-1527</orcidid></search><sort><creationdate>202305</creationdate><title>Role of exosomal miRNA in chemotherapy resistance of Colorectal cancer: A systematic review</title><author>Maleki, Masomeh ; 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subjects Biomarkers, Tumor - metabolism
chemotherapy
colorectal cancer
Colorectal Neoplasms - drug therapy
Colorectal Neoplasms - genetics
exosome
Exosomes - genetics
Exosomes - metabolism
Exosomes - pathology
Humans
microRNAs
MicroRNAs - genetics
MicroRNAs - metabolism
RNA, Messenger - metabolism
title Role of exosomal miRNA in chemotherapy resistance of Colorectal cancer: A systematic review
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