EGFR‑associated pathways involved in traditional Chinese medicine (TCM)‑1‑induced cell growth inhibition, autophagy and apoptosis in prostate cancer
Traditional Chinese medicine (TCM) has the synergistic effect of the combination of a single ingredient and a monomer, and systemic and local therapeutic effects in cancer treatment, through which TCM is able to enhance the curative effect and reduce the side effects. The present study analyzed the...
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description | Traditional Chinese medicine (TCM) has the synergistic effect of the combination of a single ingredient and a monomer, and systemic and local therapeutic effects in cancer treatment, through which TCM is able to enhance the curative effect and reduce the side effects. The present study analyzed the effect of TCM‑1 (an anti‑cancer TCM) on prostate cancer (PCa) cell lines, and studied in detail the mechanism of cell death induced by TCM‑1 in vitro and in vivo. From the present results, it was identified for the first time, to the best of our knowledge, that TCM‑1 arrested the cell cycle at the G1 phase, decreased cell viability and increased nuclear rupture in a dose‑dependent manner; these effects finally resulted in apoptosis in PCa cells. At the molecular level, the data demonstrated that TCM‑1 competitively acted on epidermal growth factor receptor (EGFR) with EGF, and suppressed the auto‑phosphorylation and activity of EGFR. Inhibition of EGFR further suppressed the downstream phosphatidylinositol 3‑kinase (PI3K)/RAC‑α serine/threonine‑protein kinase (AKT) and RAF proto‑oncogene serine/threonine‑protein kinase/extracellular signal regulated kinase signaling pathways and resulted in a decrease in the phosphorylated‑forkhead box protein O1 (at Ser256, Thr24 and Ser319) expression level, and induced cell growth inhibition and apoptosis by regulating the expression of apoptosis‑and cell cycle‑associated genes. In addition, TCM‑1 markedly inhibited the PI3K/AKT/serine/threonine‑protein kinase mTOR signaling pathway and induced cell autophagy by downregulating the phosphorylation of p70S6K and upregulating the levels of Beclin‑1 and microtubule‑associated protein light chain‑3II. In vivo, the TCM‑1‑treated group exhibited a significant decrease in tumor volume compared with the negative control group in subcutaneous xenograft nude mice by inhibiting EGFR‑associated signaling pathways. Therefore, the bio‑functions of Chinese medicine TCM‑1 in inducing PCa cell growth inhibition, autophagy and apoptosis suggested that TCM‑1 may have clinical potential for the treatment of patients with PCa. |
doi_str_mv | 10.3892/mmr.2018.8818 |
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The present study analyzed the effect of TCM‑1 (an anti‑cancer TCM) on prostate cancer (PCa) cell lines, and studied in detail the mechanism of cell death induced by TCM‑1 in vitro and in vivo. From the present results, it was identified for the first time, to the best of our knowledge, that TCM‑1 arrested the cell cycle at the G1 phase, decreased cell viability and increased nuclear rupture in a dose‑dependent manner; these effects finally resulted in apoptosis in PCa cells. At the molecular level, the data demonstrated that TCM‑1 competitively acted on epidermal growth factor receptor (EGFR) with EGF, and suppressed the auto‑phosphorylation and activity of EGFR. Inhibition of EGFR further suppressed the downstream phosphatidylinositol 3‑kinase (PI3K)/RAC‑α serine/threonine‑protein kinase (AKT) and RAF proto‑oncogene serine/threonine‑protein kinase/extracellular signal regulated kinase signaling pathways and resulted in a decrease in the phosphorylated‑forkhead box protein O1 (at Ser256, Thr24 and Ser319) expression level, and induced cell growth inhibition and apoptosis by regulating the expression of apoptosis‑and cell cycle‑associated genes. In addition, TCM‑1 markedly inhibited the PI3K/AKT/serine/threonine‑protein kinase mTOR signaling pathway and induced cell autophagy by downregulating the phosphorylation of p70S6K and upregulating the levels of Beclin‑1 and microtubule‑associated protein light chain‑3II. In vivo, the TCM‑1‑treated group exhibited a significant decrease in tumor volume compared with the negative control group in subcutaneous xenograft nude mice by inhibiting EGFR‑associated signaling pathways. Therefore, the bio‑functions of Chinese medicine TCM‑1 in inducing PCa cell growth inhibition, autophagy and apoptosis suggested that TCM‑1 may have clinical potential for the treatment of patients with PCa.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2018.8818</identifier><identifier>PMID: 29620175</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>1-Phosphatidylinositol 3-kinase ; AKT protein ; Animals ; Apoptosis ; Apoptosis - drug effects ; Autophagy ; Autophagy - drug effects ; Care and treatment ; Cell cycle ; Cell Cycle - drug effects ; Cell death ; Cell growth ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cellular signal transduction ; Cyclin D1 - metabolism ; Cyclin-dependent kinases ; Development and progression ; Epidermal growth factor ; Epidermal growth factor receptors ; Forkhead protein ; G1 phase ; Genetic aspects ; Health aspects ; Humans ; Immunohistochemistry ; Kinases ; Male ; Medicine, Chinese ; Medicine, Chinese Traditional ; Methods ; Mice ; Patient outcomes ; Phagocytosis ; Phosphatidylinositol 3-Kinase - metabolism ; Phosphorylation ; Prostate cancer ; Prostatic Neoplasms - metabolism ; Protein kinase ; Proto-Oncogene Proteins c-akt - metabolism ; Raf protein ; Receptor, Epidermal Growth Factor - metabolism ; Signal Transduction ; Threonine ; TOR protein ; Traditional Chinese medicine ; Tumor cell lines ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism ; Xenografts</subject><ispartof>Molecular medicine reports, 2018-06, Vol.17 (6), p.7875-7885</ispartof><rights>COPYRIGHT 2018 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2018</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-fa960d86c460cc9e8227879f7fdba939fff519dcc5a48ed66bc54439475659843</citedby><cites>FETCH-LOGICAL-c427t-fa960d86c460cc9e8227879f7fdba939fff519dcc5a48ed66bc54439475659843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29620175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Zhaomeng</creatorcontrib><creatorcontrib>Zhu, Qingyi</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Yin, Yingying</creatorcontrib><creatorcontrib>Kang, Dan</creatorcontrib><creatorcontrib>Cao, Runyi</creatorcontrib><creatorcontrib>Tian, Qian</creatorcontrib><creatorcontrib>Lu, Shan</creatorcontrib><creatorcontrib>Liu, Ping</creatorcontrib><title>EGFR‑associated pathways involved in traditional Chinese medicine (TCM)‑1‑induced cell growth inhibition, autophagy and apoptosis in prostate cancer</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>Traditional Chinese medicine (TCM) has the synergistic effect of the combination of a single ingredient and a monomer, and systemic and local therapeutic effects in cancer treatment, through which TCM is able to enhance the curative effect and reduce the side effects. The present study analyzed the effect of TCM‑1 (an anti‑cancer TCM) on prostate cancer (PCa) cell lines, and studied in detail the mechanism of cell death induced by TCM‑1 in vitro and in vivo. From the present results, it was identified for the first time, to the best of our knowledge, that TCM‑1 arrested the cell cycle at the G1 phase, decreased cell viability and increased nuclear rupture in a dose‑dependent manner; these effects finally resulted in apoptosis in PCa cells. At the molecular level, the data demonstrated that TCM‑1 competitively acted on epidermal growth factor receptor (EGFR) with EGF, and suppressed the auto‑phosphorylation and activity of EGFR. Inhibition of EGFR further suppressed the downstream phosphatidylinositol 3‑kinase (PI3K)/RAC‑α serine/threonine‑protein kinase (AKT) and RAF proto‑oncogene serine/threonine‑protein kinase/extracellular signal regulated kinase signaling pathways and resulted in a decrease in the phosphorylated‑forkhead box protein O1 (at Ser256, Thr24 and Ser319) expression level, and induced cell growth inhibition and apoptosis by regulating the expression of apoptosis‑and cell cycle‑associated genes. In addition, TCM‑1 markedly inhibited the PI3K/AKT/serine/threonine‑protein kinase mTOR signaling pathway and induced cell autophagy by downregulating the phosphorylation of p70S6K and upregulating the levels of Beclin‑1 and microtubule‑associated protein light chain‑3II. In vivo, the TCM‑1‑treated group exhibited a significant decrease in tumor volume compared with the negative control group in subcutaneous xenograft nude mice by inhibiting EGFR‑associated signaling pathways. Therefore, the bio‑functions of Chinese medicine TCM‑1 in inducing PCa cell growth inhibition, autophagy and apoptosis suggested that TCM‑1 may have clinical potential for the treatment of patients with PCa.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>AKT protein</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Autophagy</subject><subject>Autophagy - drug effects</subject><subject>Care and treatment</subject><subject>Cell cycle</subject><subject>Cell Cycle - drug effects</subject><subject>Cell death</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cellular signal transduction</subject><subject>Cyclin D1 - metabolism</subject><subject>Cyclin-dependent kinases</subject><subject>Development and progression</subject><subject>Epidermal growth factor</subject><subject>Epidermal growth factor receptors</subject><subject>Forkhead protein</subject><subject>G1 phase</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kinases</subject><subject>Male</subject><subject>Medicine, Chinese</subject><subject>Medicine, Chinese Traditional</subject><subject>Methods</subject><subject>Mice</subject><subject>Patient outcomes</subject><subject>Phagocytosis</subject><subject>Phosphatidylinositol 3-Kinase - metabolism</subject><subject>Phosphorylation</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Protein kinase</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Raf protein</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Signal Transduction</subject><subject>Threonine</subject><subject>TOR protein</subject><subject>Traditional Chinese medicine</subject><subject>Tumor cell lines</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>Xenografts</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptks-KFDEQxhtR3HX16FUCXlawxyTd6STHZdhdhRVB1nPI5M9Mlu6k7aR3mZuv4NXH80msdkdFkRBSFL-vqvhSVfWc4FUjJH0zDNOKYiJWQhDxoDomXJK6wbh9eIiplPyoepLzDcYdo0w-ro6o7EDD2XH17fzy4uP3L191zskEXZxFoy67O73PKMTb1N9CJkRUJm1DCSnqHq13Ibrs0OBsMBCi0-v1-1dQhMAN0c4GNMb1PdpO6a7sQL8Lm5_q10jPJY07vd0jHS3SYxpLymFphsYp5QIjIKOjcdPT6pHXfXbPDu9J9eni_Hr9tr76cPlufXZVm5byUnstO2xFZ9oOGyOdoJQLLj33dqNlI733jEhrDNOtcLbrNoa1bSNbzjomRducVKf3daH_59nlooaQl_F1dGnOimJKScPAMUBf_oPepHkCTxaqEYxJwpo_1Fb3ToXoE7hnlqLqjLWE844QCtTqPxQc64ZgUnQ-QP4vQX0vMOBTnpxX4xQGPe0VwWrZBQW7oJZdUMsuAP_iMOy8ga_6Tf_6_OYHyjiyiw</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Wu, Zhaomeng</creator><creator>Zhu, Qingyi</creator><creator>Zhang, Yu</creator><creator>Yin, Yingying</creator><creator>Kang, Dan</creator><creator>Cao, Runyi</creator><creator>Tian, Qian</creator><creator>Lu, Shan</creator><creator>Liu, Ping</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180601</creationdate><title>EGFR‑associated pathways involved in traditional Chinese medicine (TCM)‑1‑induced cell growth inhibition, autophagy and apoptosis in prostate cancer</title><author>Wu, Zhaomeng ; Zhu, Qingyi ; Zhang, Yu ; Yin, Yingying ; Kang, Dan ; Cao, Runyi ; Tian, Qian ; Lu, Shan ; Liu, Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-fa960d86c460cc9e8227879f7fdba939fff519dcc5a48ed66bc54439475659843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>AKT protein</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Autophagy</topic><topic>Autophagy - drug effects</topic><topic>Care and treatment</topic><topic>Cell cycle</topic><topic>Cell Cycle - drug effects</topic><topic>Cell death</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cellular signal transduction</topic><topic>Cyclin D1 - metabolism</topic><topic>Cyclin-dependent kinases</topic><topic>Development and progression</topic><topic>Epidermal growth factor</topic><topic>Epidermal growth factor receptors</topic><topic>Forkhead protein</topic><topic>G1 phase</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kinases</topic><topic>Male</topic><topic>Medicine, Chinese</topic><topic>Medicine, Chinese Traditional</topic><topic>Methods</topic><topic>Mice</topic><topic>Patient outcomes</topic><topic>Phagocytosis</topic><topic>Phosphatidylinositol 3-Kinase - metabolism</topic><topic>Phosphorylation</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Protein kinase</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Raf protein</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Signal Transduction</topic><topic>Threonine</topic><topic>TOR protein</topic><topic>Traditional Chinese medicine</topic><topic>Tumor cell lines</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>Xenografts</topic><toplevel>online_resources</toplevel><creatorcontrib>Wu, Zhaomeng</creatorcontrib><creatorcontrib>Zhu, Qingyi</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Yin, Yingying</creatorcontrib><creatorcontrib>Kang, Dan</creatorcontrib><creatorcontrib>Cao, Runyi</creatorcontrib><creatorcontrib>Tian, Qian</creatorcontrib><creatorcontrib>Lu, Shan</creatorcontrib><creatorcontrib>Liu, Ping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular medicine reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Zhaomeng</au><au>Zhu, Qingyi</au><au>Zhang, Yu</au><au>Yin, Yingying</au><au>Kang, Dan</au><au>Cao, Runyi</au><au>Tian, Qian</au><au>Lu, Shan</au><au>Liu, Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EGFR‑associated pathways involved in traditional Chinese medicine (TCM)‑1‑induced cell growth inhibition, autophagy and apoptosis in prostate cancer</atitle><jtitle>Molecular medicine reports</jtitle><addtitle>Mol Med Rep</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>17</volume><issue>6</issue><spage>7875</spage><epage>7885</epage><pages>7875-7885</pages><issn>1791-2997</issn><eissn>1791-3004</eissn><abstract>Traditional Chinese medicine (TCM) has the synergistic effect of the combination of a single ingredient and a monomer, and systemic and local therapeutic effects in cancer treatment, through which TCM is able to enhance the curative effect and reduce the side effects. The present study analyzed the effect of TCM‑1 (an anti‑cancer TCM) on prostate cancer (PCa) cell lines, and studied in detail the mechanism of cell death induced by TCM‑1 in vitro and in vivo. From the present results, it was identified for the first time, to the best of our knowledge, that TCM‑1 arrested the cell cycle at the G1 phase, decreased cell viability and increased nuclear rupture in a dose‑dependent manner; these effects finally resulted in apoptosis in PCa cells. At the molecular level, the data demonstrated that TCM‑1 competitively acted on epidermal growth factor receptor (EGFR) with EGF, and suppressed the auto‑phosphorylation and activity of EGFR. Inhibition of EGFR further suppressed the downstream phosphatidylinositol 3‑kinase (PI3K)/RAC‑α serine/threonine‑protein kinase (AKT) and RAF proto‑oncogene serine/threonine‑protein kinase/extracellular signal regulated kinase signaling pathways and resulted in a decrease in the phosphorylated‑forkhead box protein O1 (at Ser256, Thr24 and Ser319) expression level, and induced cell growth inhibition and apoptosis by regulating the expression of apoptosis‑and cell cycle‑associated genes. In addition, TCM‑1 markedly inhibited the PI3K/AKT/serine/threonine‑protein kinase mTOR signaling pathway and induced cell autophagy by downregulating the phosphorylation of p70S6K and upregulating the levels of Beclin‑1 and microtubule‑associated protein light chain‑3II. In vivo, the TCM‑1‑treated group exhibited a significant decrease in tumor volume compared with the negative control group in subcutaneous xenograft nude mice by inhibiting EGFR‑associated signaling pathways. Therefore, the bio‑functions of Chinese medicine TCM‑1 in inducing PCa cell growth inhibition, autophagy and apoptosis suggested that TCM‑1 may have clinical potential for the treatment of patients with PCa.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>29620175</pmid><doi>10.3892/mmr.2018.8818</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase AKT protein Animals Apoptosis Apoptosis - drug effects Autophagy Autophagy - drug effects Care and treatment Cell cycle Cell Cycle - drug effects Cell death Cell growth Cell Line, Tumor Cell Proliferation - drug effects Cell Survival - drug effects Cellular signal transduction Cyclin D1 - metabolism Cyclin-dependent kinases Development and progression Epidermal growth factor Epidermal growth factor receptors Forkhead protein G1 phase Genetic aspects Health aspects Humans Immunohistochemistry Kinases Male Medicine, Chinese Medicine, Chinese Traditional Methods Mice Patient outcomes Phagocytosis Phosphatidylinositol 3-Kinase - metabolism Phosphorylation Prostate cancer Prostatic Neoplasms - metabolism Protein kinase Proto-Oncogene Proteins c-akt - metabolism Raf protein Receptor, Epidermal Growth Factor - metabolism Signal Transduction Threonine TOR protein Traditional Chinese medicine Tumor cell lines Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism Xenografts |
title | EGFR‑associated pathways involved in traditional Chinese medicine (TCM)‑1‑induced cell growth inhibition, autophagy and apoptosis in prostate cancer |
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