Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis

Berberis amurensis Rupr. is used to treat cancer as a traditional herbal medicine. Berbamine (BBM) is a natural bisbenzylisoquinoline alkaloid extracted from Berberis amurensis which possesses multiple pharmacological activity including anticancer. To investigate the influence of BBM on the progress...

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Veröffentlicht in:Journal of ethnopharmacology 2023-03, Vol.303, p.116025-116025, Article 116025
Hauptverfasser: Liu, Lu, Liang, Dan, Zheng, Qiao, Zhao, Maoyuan, Lv, RuiTing, Tang, Jianyuan, Chen, Nianzhi
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container_title Journal of ethnopharmacology
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Liang, Dan
Zheng, Qiao
Zhao, Maoyuan
Lv, RuiTing
Tang, Jianyuan
Chen, Nianzhi
description Berberis amurensis Rupr. is used to treat cancer as a traditional herbal medicine. Berbamine (BBM) is a natural bisbenzylisoquinoline alkaloid extracted from Berberis amurensis which possesses multiple pharmacological activity including anticancer. To investigate the influence of BBM on the progression of colorectal cancer (CRC) and further explore the underlying mechanism of BBM based on the RTKs/Akt signaling pathway. In vitro, cell viability and colony formation were conducted to detect BBM inhibitory of CRC cell lines. Transwell was detected the ability of migration and invasion by BBM. Apoptosis detection assay, cell cycle assay and the measurement of ROS were detected to confirm the inductive effect of cell apoptosis. RT-qPCR and Western blot to clarify the specific mechanism of anticancer. Finally, we conducted HE staining, Ki67, Tunnel and immunochemistry were confirmed the anti-colorectal cancer activity of BBM from vivo study. We found that BBM could inhibit CRC cell lines growth. Moreover, BBM presented an inhibitory effect the ability of migration and invasion in CRC cells. Furthermore, the occurrence of apoptosis was involved in the anti-colorectal cancer role of BBM. BBM also triggered ROS accumulation in CRC cells that might be a key factor for the inductive effect of BBM in cell apoptosis. Cell cycle assay revealed that BBM induced the arrest of G1-S phase and increased the p21 levels but decreased CyclinE1, CyclinE2, CDK6, CyclinD1. RT-qPCR manifested that the down-regulation effect of BBM on AKT1, EGFR, PDGFRα and FGFR4 genes. The results also showed that BBM could decreased the expression levels of phosphor-AKT, PDGFRα, PDGFRβ, EGFR, FGFR3 and FGFR4 which belong to RTKs family. Consistently, BBM remarkably suppressed tumor xenograft growth in nude mice. Taken together, all the results as presented above suggest that BBM as a novel multitargeted receptor tyrosine kinase inhibitor plays a crucial role in the inhibitory effect of CRC and may be a promising therapeutic agent for the CRC in clinic. [Display omitted] •BBM exerts strong anti-colorectal cancer effect both in vitro and in vivo.•BBM inhibits the progression of colorectal cancer through inducing apoptosis, suppressing proliferation, migration, invasion of cells.•BBM is a novel multitargeted receptor tyrosine kinase (RTK) inhibitor from natural products. RTKs/Akt signaling pathway plays a vital role in the anti-colorectal cancer effect of BBM.
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Berbamine (BBM) is a natural bisbenzylisoquinoline alkaloid extracted from Berberis amurensis which possesses multiple pharmacological activity including anticancer. To investigate the influence of BBM on the progression of colorectal cancer (CRC) and further explore the underlying mechanism of BBM based on the RTKs/Akt signaling pathway. In vitro, cell viability and colony formation were conducted to detect BBM inhibitory of CRC cell lines. Transwell was detected the ability of migration and invasion by BBM. Apoptosis detection assay, cell cycle assay and the measurement of ROS were detected to confirm the inductive effect of cell apoptosis. RT-qPCR and Western blot to clarify the specific mechanism of anticancer. Finally, we conducted HE staining, Ki67, Tunnel and immunochemistry were confirmed the anti-colorectal cancer activity of BBM from vivo study. We found that BBM could inhibit CRC cell lines growth. Moreover, BBM presented an inhibitory effect the ability of migration and invasion in CRC cells. Furthermore, the occurrence of apoptosis was involved in the anti-colorectal cancer role of BBM. BBM also triggered ROS accumulation in CRC cells that might be a key factor for the inductive effect of BBM in cell apoptosis. Cell cycle assay revealed that BBM induced the arrest of G1-S phase and increased the p21 levels but decreased CyclinE1, CyclinE2, CDK6, CyclinD1. RT-qPCR manifested that the down-regulation effect of BBM on AKT1, EGFR, PDGFRα and FGFR4 genes. The results also showed that BBM could decreased the expression levels of phosphor-AKT, PDGFRα, PDGFRβ, EGFR, FGFR3 and FGFR4 which belong to RTKs family. Consistently, BBM remarkably suppressed tumor xenograft growth in nude mice. Taken together, all the results as presented above suggest that BBM as a novel multitargeted receptor tyrosine kinase inhibitor plays a crucial role in the inhibitory effect of CRC and may be a promising therapeutic agent for the CRC in clinic. [Display omitted] •BBM exerts strong anti-colorectal cancer effect both in vitro and in vivo.•BBM inhibits the progression of colorectal cancer through inducing apoptosis, suppressing proliferation, migration, invasion of cells.•BBM is a novel multitargeted receptor tyrosine kinase (RTK) inhibitor from natural products. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-2ee6d2c282e1ffd1bb8308fef9eaea45a1d47cc7b4b91c4af452e2352de927883</citedby><cites>FETCH-LOGICAL-c353t-2ee6d2c282e1ffd1bb8308fef9eaea45a1d47cc7b4b91c4af452e2352de927883</cites><orcidid>0000-0002-7508-6772</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378874122010649$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36496042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Liang, Dan</creatorcontrib><creatorcontrib>Zheng, Qiao</creatorcontrib><creatorcontrib>Zhao, Maoyuan</creatorcontrib><creatorcontrib>Lv, RuiTing</creatorcontrib><creatorcontrib>Tang, Jianyuan</creatorcontrib><creatorcontrib>Chen, Nianzhi</creatorcontrib><title>Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>Berberis amurensis Rupr. is used to treat cancer as a traditional herbal medicine. Berbamine (BBM) is a natural bisbenzylisoquinoline alkaloid extracted from Berberis amurensis which possesses multiple pharmacological activity including anticancer. To investigate the influence of BBM on the progression of colorectal cancer (CRC) and further explore the underlying mechanism of BBM based on the RTKs/Akt signaling pathway. In vitro, cell viability and colony formation were conducted to detect BBM inhibitory of CRC cell lines. Transwell was detected the ability of migration and invasion by BBM. Apoptosis detection assay, cell cycle assay and the measurement of ROS were detected to confirm the inductive effect of cell apoptosis. RT-qPCR and Western blot to clarify the specific mechanism of anticancer. Finally, we conducted HE staining, Ki67, Tunnel and immunochemistry were confirmed the anti-colorectal cancer activity of BBM from vivo study. We found that BBM could inhibit CRC cell lines growth. Moreover, BBM presented an inhibitory effect the ability of migration and invasion in CRC cells. Furthermore, the occurrence of apoptosis was involved in the anti-colorectal cancer role of BBM. BBM also triggered ROS accumulation in CRC cells that might be a key factor for the inductive effect of BBM in cell apoptosis. Cell cycle assay revealed that BBM induced the arrest of G1-S phase and increased the p21 levels but decreased CyclinE1, CyclinE2, CDK6, CyclinD1. RT-qPCR manifested that the down-regulation effect of BBM on AKT1, EGFR, PDGFRα and FGFR4 genes. The results also showed that BBM could decreased the expression levels of phosphor-AKT, PDGFRα, PDGFRβ, EGFR, FGFR3 and FGFR4 which belong to RTKs family. Consistently, BBM remarkably suppressed tumor xenograft growth in nude mice. Taken together, all the results as presented above suggest that BBM as a novel multitargeted receptor tyrosine kinase inhibitor plays a crucial role in the inhibitory effect of CRC and may be a promising therapeutic agent for the CRC in clinic. [Display omitted] •BBM exerts strong anti-colorectal cancer effect both in vitro and in vivo.•BBM inhibits the progression of colorectal cancer through inducing apoptosis, suppressing proliferation, migration, invasion of cells.•BBM is a novel multitargeted receptor tyrosine kinase (RTK) inhibitor from natural products. RTKs/Akt signaling pathway plays a vital role in the anti-colorectal cancer effect of BBM.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Benzylisoquinolines - pharmacology</subject><subject>Benzylisoquinolines - therapeutic use</subject><subject>Berbamine dihydrochloride</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - pathology</subject><subject>ErbB Receptors - metabolism</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Reactive Oxygen Species</subject><subject>Receptor, Platelet-Derived Growth Factor alpha</subject><subject>RTKs/Akt pathway</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAWyQl2zS-pU4EatS8RKVkFBZsbAce0Jd0jrYaUX_nlQtLFmNRjr3auYgdEnJkBKajRbDBTRDRhgbUpoRlh6hPs0lS2Qq-THqEy7zJJeC9tBZjAtCiKSCnKIez0SREcH66P0WQqmXbgXYuvnWBm_mtQ_OAo7rpgkQI0TczgE3wX_sVudX2FfY-A4D0-oaG70yEPDGafw6e46j8WeL9beL5-ik0nWEi8McoLf7u9nkMZm-PDxNxtPE8JS3CQPILDMsZ0CrytKyzDnJK6gK0KBFqqkV0hhZirKgRuhKpAwYT5mFgsk85wN0ve_tTvxaQ2zV0kUDda1X4NdRMZlyVshCig6le9QEH2OASjXBLXXYKkrUzqlaqM6p2jlVe6dd5upQvy6XYP8SvxI74GYPQPfkxkFQ0TjonFi3M6Ssd__U_wAB24iX</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Liu, Lu</creator><creator>Liang, Dan</creator><creator>Zheng, Qiao</creator><creator>Zhao, Maoyuan</creator><creator>Lv, RuiTing</creator><creator>Tang, Jianyuan</creator><creator>Chen, Nianzhi</creator><general>Elsevier B.V</general><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/0000-0002-7508-6772</orcidid></search><sort><creationdate>20230301</creationdate><title>Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis</title><author>Liu, Lu ; Liang, Dan ; Zheng, Qiao ; Zhao, Maoyuan ; Lv, RuiTing ; Tang, Jianyuan ; Chen, Nianzhi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-2ee6d2c282e1ffd1bb8308fef9eaea45a1d47cc7b4b91c4af452e2352de927883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Benzylisoquinolines - pharmacology</topic><topic>Benzylisoquinolines - therapeutic use</topic><topic>Berbamine dihydrochloride</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - pathology</topic><topic>ErbB Receptors - metabolism</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Reactive Oxygen Species</topic><topic>Receptor, Platelet-Derived Growth Factor alpha</topic><topic>RTKs/Akt pathway</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Liang, Dan</creatorcontrib><creatorcontrib>Zheng, Qiao</creatorcontrib><creatorcontrib>Zhao, Maoyuan</creatorcontrib><creatorcontrib>Lv, RuiTing</creatorcontrib><creatorcontrib>Tang, Jianyuan</creatorcontrib><creatorcontrib>Chen, Nianzhi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Lu</au><au>Liang, Dan</au><au>Zheng, Qiao</au><au>Zhao, Maoyuan</au><au>Lv, RuiTing</au><au>Tang, Jianyuan</au><au>Chen, Nianzhi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2023-03-01</date><risdate>2023</risdate><volume>303</volume><spage>116025</spage><epage>116025</epage><pages>116025-116025</pages><artnum>116025</artnum><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>Berberis amurensis Rupr. is used to treat cancer as a traditional herbal medicine. Berbamine (BBM) is a natural bisbenzylisoquinoline alkaloid extracted from Berberis amurensis which possesses multiple pharmacological activity including anticancer. To investigate the influence of BBM on the progression of colorectal cancer (CRC) and further explore the underlying mechanism of BBM based on the RTKs/Akt signaling pathway. In vitro, cell viability and colony formation were conducted to detect BBM inhibitory of CRC cell lines. Transwell was detected the ability of migration and invasion by BBM. Apoptosis detection assay, cell cycle assay and the measurement of ROS were detected to confirm the inductive effect of cell apoptosis. RT-qPCR and Western blot to clarify the specific mechanism of anticancer. Finally, we conducted HE staining, Ki67, Tunnel and immunochemistry were confirmed the anti-colorectal cancer activity of BBM from vivo study. We found that BBM could inhibit CRC cell lines growth. Moreover, BBM presented an inhibitory effect the ability of migration and invasion in CRC cells. Furthermore, the occurrence of apoptosis was involved in the anti-colorectal cancer role of BBM. BBM also triggered ROS accumulation in CRC cells that might be a key factor for the inductive effect of BBM in cell apoptosis. Cell cycle assay revealed that BBM induced the arrest of G1-S phase and increased the p21 levels but decreased CyclinE1, CyclinE2, CDK6, CyclinD1. RT-qPCR manifested that the down-regulation effect of BBM on AKT1, EGFR, PDGFRα and FGFR4 genes. The results also showed that BBM could decreased the expression levels of phosphor-AKT, PDGFRα, PDGFRβ, EGFR, FGFR3 and FGFR4 which belong to RTKs family. Consistently, BBM remarkably suppressed tumor xenograft growth in nude mice. Taken together, all the results as presented above suggest that BBM as a novel multitargeted receptor tyrosine kinase inhibitor plays a crucial role in the inhibitory effect of CRC and may be a promising therapeutic agent for the CRC in clinic. [Display omitted] •BBM exerts strong anti-colorectal cancer effect both in vitro and in vivo.•BBM inhibits the progression of colorectal cancer through inducing apoptosis, suppressing proliferation, migration, invasion of cells.•BBM is a novel multitargeted receptor tyrosine kinase (RTK) inhibitor from natural products. RTKs/Akt signaling pathway plays a vital role in the anti-colorectal cancer effect of BBM.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>36496042</pmid><doi>10.1016/j.jep.2022.116025</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7508-6772</orcidid></addata></record>
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subjects Animals
Apoptosis
Benzylisoquinolines - pharmacology
Benzylisoquinolines - therapeutic use
Berbamine dihydrochloride
Cell Line, Tumor
Cell Movement
Cell Proliferation
Colorectal cancer
Colorectal Neoplasms - pathology
ErbB Receptors - metabolism
Humans
Mice
Mice, Nude
Proto-Oncogene Proteins c-akt - metabolism
Reactive Oxygen Species
Receptor, Platelet-Derived Growth Factor alpha
RTKs/Akt pathway
title Berbamine dihydrochloride suppresses the progression of colorectal cancer via RTKs/Akt axis
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