HnRNPAB is an independent prognostic factor in non‑small cell lung cancer and is involved in cell proliferation and metastasis
Heterogeneous nuclear ribonucleoprotein A/B (hnRNPAB) is an RNA binding protein that is closely associated with the biological function and metabolism of RNA, which is involved in the malignant transformation of various tumor cells. However, the role and mechanisms of hnRNPAB in non-small cell lung...
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Veröffentlicht in: | Oncology letters 2023-06, Vol.25 (6), p.215, Article 215 |
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description | Heterogeneous nuclear ribonucleoprotein A/B (hnRNPAB) is an RNA binding protein that is closely associated with the biological function and metabolism of RNA, which is involved in the malignant transformation of various tumor cells. However, the role and mechanisms of hnRNPAB in non-small cell lung cancer (NSCLC) are still unclear. In the present study, the expression levels of hnRNPAB in NSCLC and normal tissues were analyzed using the human protein atlas database and UALCAN database. The clinical significance of hnRNPAB was assayed using the data of NSCLC cases from The Cancer Genome Atlas database. Subsequently, two stable NSCLC cell lines with hnRNPAB knockdown were constructed and the effects of hnRNPAB silencing on cell viability, migration, invasion and epithelial-mesenchymal transition (EMT) were identified. Genes associated with hnRNPAB expression in NSCLC were screened using the Linked Omics database and verified by quantitative real-time PCR (RT-qPCR). The database analysis indicated that hnRNPAB was mainly expressed in the nucleus of NSCLC cells. Compared with the normal tissues, hnRNPAB expression was overexpressed in NSCLC tissues and was closely associated with the overall survival, sex, tumor-node-metastases classification, and poor prognosis of patients with lung adenocarcinoma. Functionally, knockdown of hnRNPAB inhibited the proliferation, migration, invasion and EMT of NSCLC cells and arrested the cell cycle at G
phase. Mechanistically, the bioinformatics analysis and RT-qPCR verification demonstrated that hnRNPAB knockdown led to a significant expression change of genes associated with tumorigenesis. In conclusion, the present study indicated that hnRNPAB played an important role in the malignant transformation of NSCLC, supporting the significance of hnRNPAB as a novel potential therapeutic target for the early diagnosis and prognosis of NSCLC. |
doi_str_mv | 10.3892/ol.2023.13801 |
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phase. Mechanistically, the bioinformatics analysis and RT-qPCR verification demonstrated that hnRNPAB knockdown led to a significant expression change of genes associated with tumorigenesis. In conclusion, the present study indicated that hnRNPAB played an important role in the malignant transformation of NSCLC, supporting the significance of hnRNPAB as a novel potential therapeutic target for the early diagnosis and prognosis of NSCLC.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2023.13801</identifier><identifier>PMID: 37153057</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Biomarkers ; Cancer ; Cell cycle ; Cell growth ; Ethylenediaminetetraacetic acid ; Genetic aspects ; Genomes ; Genomics ; Health aspects ; Infections ; Liver cancer ; Localization ; Lung cancer ; Lung cancer, Non-small cell ; Lung cancer, Small cell ; Medical prognosis ; Metastasis ; Prognosis ; Protein binding ; Reagents ; RNA</subject><ispartof>Oncology letters, 2023-06, Vol.25 (6), p.215, Article 215</ispartof><rights>Copyright: © Wang et al.</rights><rights>COPYRIGHT 2023 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2023</rights><rights>Copyright: © Wang et al. 2023</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157350/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157350/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37153057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Qinrong</creatorcontrib><creatorcontrib>Gou, Xuanjing</creatorcontrib><creatorcontrib>Liu, Lingling</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Yuan, Hang</creatorcontrib><creatorcontrib>Zhao, Yan</creatorcontrib><creatorcontrib>Xie, Yuan</creatorcontrib><creatorcontrib>Zhou, Jianjiang</creatorcontrib><creatorcontrib>Song, Kewei</creatorcontrib><title>HnRNPAB is an independent prognostic factor in non‑small cell lung cancer and is involved in cell proliferation and metastasis</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Heterogeneous nuclear ribonucleoprotein A/B (hnRNPAB) is an RNA binding protein that is closely associated with the biological function and metabolism of RNA, which is involved in the malignant transformation of various tumor cells. However, the role and mechanisms of hnRNPAB in non-small cell lung cancer (NSCLC) are still unclear. In the present study, the expression levels of hnRNPAB in NSCLC and normal tissues were analyzed using the human protein atlas database and UALCAN database. The clinical significance of hnRNPAB was assayed using the data of NSCLC cases from The Cancer Genome Atlas database. Subsequently, two stable NSCLC cell lines with hnRNPAB knockdown were constructed and the effects of hnRNPAB silencing on cell viability, migration, invasion and epithelial-mesenchymal transition (EMT) were identified. Genes associated with hnRNPAB expression in NSCLC were screened using the Linked Omics database and verified by quantitative real-time PCR (RT-qPCR). The database analysis indicated that hnRNPAB was mainly expressed in the nucleus of NSCLC cells. Compared with the normal tissues, hnRNPAB expression was overexpressed in NSCLC tissues and was closely associated with the overall survival, sex, tumor-node-metastases classification, and poor prognosis of patients with lung adenocarcinoma. Functionally, knockdown of hnRNPAB inhibited the proliferation, migration, invasion and EMT of NSCLC cells and arrested the cell cycle at G
phase. Mechanistically, the bioinformatics analysis and RT-qPCR verification demonstrated that hnRNPAB knockdown led to a significant expression change of genes associated with tumorigenesis. In conclusion, the present study indicated that hnRNPAB played an important role in the malignant transformation of NSCLC, supporting the significance of hnRNPAB as a novel potential therapeutic target for the early diagnosis and prognosis of NSCLC.</description><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Infections</subject><subject>Liver cancer</subject><subject>Localization</subject><subject>Lung cancer</subject><subject>Lung cancer, Non-small cell</subject><subject>Lung cancer, Small cell</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Prognosis</subject><subject>Protein binding</subject><subject>Reagents</subject><subject>RNA</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkttqFDEYgAex2FJ76a0MCN7NmsPkMFeyFrVCsUX0OvybyeymZJI1mVnoXV_BV_RJzGzrugulmIQkJF--nP6ieIXRjMqGvAtuRhChM0wlws-KEywaUmEkyfNdX9THxVlKNygnxrGU_EVxTAVmFDFxUtxd-G9fr-cfSptK8KX1rVmbXPmhXMew9CENVpcd6CHEPFv64H_f_Uo9OFdqkys3-mWpwWsTs6CdPNZvgtuYduK3TDY525kIgw1-S_VmgJSLTS-Low5cMmcP7Wnx49PH7-cX1eXV5y_n88tKMy6HChoqa60ZBs1EvSCsrk2ncQPAOOGiwbLl0MCiqylkrtNGtlQuhGhBSkMEPS3e33vX46I3rc43jODUOtoe4q0KYNXhjLcrtQwbhRFmgjKUDW8eDDH8HE0a1E0Yo8-HVkTm164pZ-QftQRnlPVdyDbd26TVXHCCak4pe5pihDSE08k1e4TKuTW91cGbzubxA-3_Ldjb4e3egpUBN6xScOP0UenQ_DS4Z6zuQR1DStF0uyfGSE1Bq4JTU9CqbdBm_vX-v-zovyFK_wDX7uYE</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Wang, Qinrong</creator><creator>Gou, Xuanjing</creator><creator>Liu, Lingling</creator><creator>Zhang, Ting</creator><creator>Yuan, Hang</creator><creator>Zhao, Yan</creator><creator>Xie, Yuan</creator><creator>Zhou, Jianjiang</creator><creator>Song, Kewei</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20230601</creationdate><title>HnRNPAB is an independent prognostic factor in non‑small cell lung cancer and is involved in cell proliferation and metastasis</title><author>Wang, Qinrong ; Gou, Xuanjing ; Liu, Lingling ; Zhang, Ting ; Yuan, Hang ; Zhao, Yan ; Xie, Yuan ; Zhou, Jianjiang ; Song, Kewei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c568t-a9384cc51ac574b2544efc19aa56267918d6a9abf43a4ccfce8d38b77da88e273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biomarkers</topic><topic>Cancer</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>Infections</topic><topic>Liver cancer</topic><topic>Localization</topic><topic>Lung cancer</topic><topic>Lung cancer, Non-small cell</topic><topic>Lung cancer, Small cell</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Prognosis</topic><topic>Protein binding</topic><topic>Reagents</topic><topic>RNA</topic><toplevel>online_resources</toplevel><creatorcontrib>Wang, Qinrong</creatorcontrib><creatorcontrib>Gou, Xuanjing</creatorcontrib><creatorcontrib>Liu, Lingling</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Yuan, Hang</creatorcontrib><creatorcontrib>Zhao, Yan</creatorcontrib><creatorcontrib>Xie, Yuan</creatorcontrib><creatorcontrib>Zhou, Jianjiang</creatorcontrib><creatorcontrib>Song, Kewei</creatorcontrib><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>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</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qinrong</au><au>Gou, Xuanjing</au><au>Liu, Lingling</au><au>Zhang, Ting</au><au>Yuan, Hang</au><au>Zhao, Yan</au><au>Xie, Yuan</au><au>Zhou, Jianjiang</au><au>Song, Kewei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HnRNPAB is an independent prognostic factor in non‑small cell lung cancer and is involved in cell proliferation and metastasis</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>25</volume><issue>6</issue><spage>215</spage><pages>215-</pages><artnum>215</artnum><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Heterogeneous nuclear ribonucleoprotein A/B (hnRNPAB) is an RNA binding protein that is closely associated with the biological function and metabolism of RNA, which is involved in the malignant transformation of various tumor cells. However, the role and mechanisms of hnRNPAB in non-small cell lung cancer (NSCLC) are still unclear. In the present study, the expression levels of hnRNPAB in NSCLC and normal tissues were analyzed using the human protein atlas database and UALCAN database. The clinical significance of hnRNPAB was assayed using the data of NSCLC cases from The Cancer Genome Atlas database. Subsequently, two stable NSCLC cell lines with hnRNPAB knockdown were constructed and the effects of hnRNPAB silencing on cell viability, migration, invasion and epithelial-mesenchymal transition (EMT) were identified. Genes associated with hnRNPAB expression in NSCLC were screened using the Linked Omics database and verified by quantitative real-time PCR (RT-qPCR). The database analysis indicated that hnRNPAB was mainly expressed in the nucleus of NSCLC cells. Compared with the normal tissues, hnRNPAB expression was overexpressed in NSCLC tissues and was closely associated with the overall survival, sex, tumor-node-metastases classification, and poor prognosis of patients with lung adenocarcinoma. Functionally, knockdown of hnRNPAB inhibited the proliferation, migration, invasion and EMT of NSCLC cells and arrested the cell cycle at G
phase. Mechanistically, the bioinformatics analysis and RT-qPCR verification demonstrated that hnRNPAB knockdown led to a significant expression change of genes associated with tumorigenesis. In conclusion, the present study indicated that hnRNPAB played an important role in the malignant transformation of NSCLC, supporting the significance of hnRNPAB as a novel potential therapeutic target for the early diagnosis and prognosis of NSCLC.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>37153057</pmid><doi>10.3892/ol.2023.13801</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Cancer Cell cycle Cell growth Ethylenediaminetetraacetic acid Genetic aspects Genomes Genomics Health aspects Infections Liver cancer Localization Lung cancer Lung cancer, Non-small cell Lung cancer, Small cell Medical prognosis Metastasis Prognosis Protein binding Reagents RNA |
title | HnRNPAB is an independent prognostic factor in non‑small cell lung cancer and is involved in cell proliferation and metastasis |
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