Global gene expression differentiating pure bronchioloalveolar carcinoma from adenocarcinoma with bronchioloalveolar carcinoma features

OBJECTIVES Pure bronchioloalveolar carcinoma (BAC) is considered the early stage of lung adenocarcinoma, and is even regarded as lung adenocarcinoma in situ. This study was designed to investigate the differences in the gene expression of pure BAC and that of adenocarcinoma with bronchioloalveolar f...

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Veröffentlicht in:European journal of cardio-thoracic surgery 2013-04, Vol.43 (4), p.765-771
Hauptverfasser: Zhang, Wen-Cheng, Zhang, Zhen-Fa, You, Jian, Wang, Chang-Li
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creator Zhang, Wen-Cheng
Zhang, Zhen-Fa
You, Jian
Wang, Chang-Li
description OBJECTIVES Pure bronchioloalveolar carcinoma (BAC) is considered the early stage of lung adenocarcinoma, and is even regarded as lung adenocarcinoma in situ. This study was designed to investigate the differences in the gene expression of pure BAC and that of adenocarcinoma with bronchioloalveolar features and explore the mechanism of BAC progression to adenocarcinoma with bronchioloalveolar features METHODS Total RNA was extracted from 16 tissue specimens. Expression analysis was carried out using Agilent 4 × 44 k arrays. Gene ontology analysis was used to define pathways altered in bronchioloalveolar progression. Differentially expressed candidate genes were validated using quantitative real-time PCR. The statistical analysis was carried out according to the methods of the paired t-test. RESULTS Adenocarcinoma with bronchioloalveolar features demonstrated an increased expression of 23 genes and reduced expression of 20 genes compared with BAC. These genes were considered candidate marker genes for tumour progression and metastasis. Genes overexpressed in adenocarcinoma with bronchioloalveolar features included fibroblast growth factor receptor 1, and CLDN18 (claudin 18), whereas those overexpressed in BAC included ataxia telangiectasia and Rad3 related (ataxia telangiectasia mutated and Rad3-related), and activating transcription factor 2. Mitogen-activated protein kinase (MAPK) pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with pure BAC. CONCLUSIONS Microarray-based expression profiling revealed interesting novel candidate genes in BAC and adenocarcinoma with bronchioloalveolar features. The MAPK pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with the pure BAC pathway, which is worthy of being explored because it could partially explain the mechanism of the progression of BAC to adenocarcinoma with bronchioloalveolar features.
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This study was designed to investigate the differences in the gene expression of pure BAC and that of adenocarcinoma with bronchioloalveolar features and explore the mechanism of BAC progression to adenocarcinoma with bronchioloalveolar features METHODS Total RNA was extracted from 16 tissue specimens. Expression analysis was carried out using Agilent 4 × 44 k arrays. Gene ontology analysis was used to define pathways altered in bronchioloalveolar progression. Differentially expressed candidate genes were validated using quantitative real-time PCR. The statistical analysis was carried out according to the methods of the paired t-test. RESULTS Adenocarcinoma with bronchioloalveolar features demonstrated an increased expression of 23 genes and reduced expression of 20 genes compared with BAC. These genes were considered candidate marker genes for tumour progression and metastasis. Genes overexpressed in adenocarcinoma with bronchioloalveolar features included fibroblast growth factor receptor 1, and CLDN18 (claudin 18), whereas those overexpressed in BAC included ataxia telangiectasia and Rad3 related (ataxia telangiectasia mutated and Rad3-related), and activating transcription factor 2. Mitogen-activated protein kinase (MAPK) pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with pure BAC. CONCLUSIONS Microarray-based expression profiling revealed interesting novel candidate genes in BAC and adenocarcinoma with bronchioloalveolar features. The MAPK pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with the pure BAC pathway, which is worthy of being explored because it could partially explain the mechanism of the progression of BAC to adenocarcinoma with bronchioloalveolar features.</description><identifier>ISSN: 1010-7940</identifier><identifier>EISSN: 1873-734X</identifier><identifier>DOI: 10.1093/ejcts/ezs427</identifier><identifier>PMID: 22864788</identifier><language>eng</language><publisher>Germany: Oxford University Press</publisher><subject>Adenocarcinoma - chemistry ; Adenocarcinoma - classification ; Adenocarcinoma - diagnosis ; Adenocarcinoma - metabolism ; Adenocarcinoma of Lung ; Adenocarcinoma, Bronchiolo-Alveolar - classification ; Adenocarcinoma, Bronchiolo-Alveolar - diagnosis ; Adenocarcinoma, Bronchiolo-Alveolar - genetics ; Adenocarcinoma, Bronchiolo-Alveolar - metabolism ; Aged ; Aged, 80 and over ; Diagnosis, Differential ; Female ; Gene Expression Profiling ; Humans ; Lung Neoplasms - chemistry ; Lung Neoplasms - classification ; Lung Neoplasms - diagnosis ; Lung Neoplasms - genetics ; Lung Neoplasms - metabolism ; Male ; Middle Aged ; Neoplasm Proteins - biosynthesis ; Neoplasm Proteins - genetics ; Neoplasm Staging ; Oligonucleotide Array Sequence Analysis ; Real-Time Polymerase Chain Reaction ; RNA, Messenger - analysis ; RNA, Messenger - metabolism</subject><ispartof>European journal of cardio-thoracic surgery, 2013-04, Vol.43 (4), p.765-771</ispartof><rights>The Author 2012. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c318t-f297cfda7973248186b828be4100125ba72e3a9322857e9b2b76417fc74e4a013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22864788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Wen-Cheng</creatorcontrib><creatorcontrib>Zhang, Zhen-Fa</creatorcontrib><creatorcontrib>You, Jian</creatorcontrib><creatorcontrib>Wang, Chang-Li</creatorcontrib><title>Global gene expression differentiating pure bronchioloalveolar carcinoma from adenocarcinoma with bronchioloalveolar carcinoma features</title><title>European journal of cardio-thoracic surgery</title><addtitle>Eur J Cardiothorac Surg</addtitle><description>OBJECTIVES Pure bronchioloalveolar carcinoma (BAC) is considered the early stage of lung adenocarcinoma, and is even regarded as lung adenocarcinoma in situ. This study was designed to investigate the differences in the gene expression of pure BAC and that of adenocarcinoma with bronchioloalveolar features and explore the mechanism of BAC progression to adenocarcinoma with bronchioloalveolar features METHODS Total RNA was extracted from 16 tissue specimens. Expression analysis was carried out using Agilent 4 × 44 k arrays. Gene ontology analysis was used to define pathways altered in bronchioloalveolar progression. Differentially expressed candidate genes were validated using quantitative real-time PCR. The statistical analysis was carried out according to the methods of the paired t-test. RESULTS Adenocarcinoma with bronchioloalveolar features demonstrated an increased expression of 23 genes and reduced expression of 20 genes compared with BAC. These genes were considered candidate marker genes for tumour progression and metastasis. Genes overexpressed in adenocarcinoma with bronchioloalveolar features included fibroblast growth factor receptor 1, and CLDN18 (claudin 18), whereas those overexpressed in BAC included ataxia telangiectasia and Rad3 related (ataxia telangiectasia mutated and Rad3-related), and activating transcription factor 2. Mitogen-activated protein kinase (MAPK) pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with pure BAC. CONCLUSIONS Microarray-based expression profiling revealed interesting novel candidate genes in BAC and adenocarcinoma with bronchioloalveolar features. The MAPK pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with the pure BAC pathway, which is worthy of being explored because it could partially explain the mechanism of the progression of BAC to adenocarcinoma with bronchioloalveolar features.</description><subject>Adenocarcinoma - chemistry</subject><subject>Adenocarcinoma - classification</subject><subject>Adenocarcinoma - diagnosis</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma of Lung</subject><subject>Adenocarcinoma, Bronchiolo-Alveolar - classification</subject><subject>Adenocarcinoma, Bronchiolo-Alveolar - diagnosis</subject><subject>Adenocarcinoma, Bronchiolo-Alveolar - genetics</subject><subject>Adenocarcinoma, Bronchiolo-Alveolar - metabolism</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Lung Neoplasms - chemistry</subject><subject>Lung Neoplasms - classification</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Staging</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><issn>1010-7940</issn><issn>1873-734X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqWwMSNvMBDqr8bOiCooSEgsILFFjnNpXSVxsBO-_gB_m0AKbDDd6fTce7oHoUNKzihJ-BTWpg1TeAuCyS00pkrySHLxsN33hJJIJoKM0F4Ia0JIzJncRSPGVCykUmP0vihdpku8hBowvDQeQrCuxrktCvBQt1a3tl7ipvOAM-9qs7KudLp8Aldqj432xtau0rjwrsI6h9r9zp5tu_pnC3TbR4d9tFPoMsDBpk7Q_eXF3fwqurldXM_PbyLDqWqjgiXSFLmWieRMKKriTDGVgaCEUDbLtGTAdcL7B2cSkoxlMhZUFkYKEJpQPkEnQ27j3WMHoU0rGwyUpa7BdSGl_ZneKueqR08H1HgXgocibbyttH9NKUk_1adf6tNBfY8fbZK7rIL8B_523QPHA-C65u-oD1_Nko0</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Zhang, Wen-Cheng</creator><creator>Zhang, Zhen-Fa</creator><creator>You, Jian</creator><creator>Wang, Chang-Li</creator><general>Oxford University Press</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></search><sort><creationdate>201304</creationdate><title>Global gene expression differentiating pure bronchioloalveolar carcinoma from adenocarcinoma with bronchioloalveolar carcinoma features</title><author>Zhang, Wen-Cheng ; Zhang, Zhen-Fa ; You, Jian ; Wang, Chang-Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c318t-f297cfda7973248186b828be4100125ba72e3a9322857e9b2b76417fc74e4a013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenocarcinoma - chemistry</topic><topic>Adenocarcinoma - classification</topic><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma of Lung</topic><topic>Adenocarcinoma, Bronchiolo-Alveolar - classification</topic><topic>Adenocarcinoma, Bronchiolo-Alveolar - diagnosis</topic><topic>Adenocarcinoma, Bronchiolo-Alveolar - genetics</topic><topic>Adenocarcinoma, Bronchiolo-Alveolar - metabolism</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Lung Neoplasms - chemistry</topic><topic>Lung Neoplasms - classification</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Staging</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wen-Cheng</creatorcontrib><creatorcontrib>Zhang, Zhen-Fa</creatorcontrib><creatorcontrib>You, Jian</creatorcontrib><creatorcontrib>Wang, Chang-Li</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>European journal of cardio-thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wen-Cheng</au><au>Zhang, Zhen-Fa</au><au>You, Jian</au><au>Wang, Chang-Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global gene expression differentiating pure bronchioloalveolar carcinoma from adenocarcinoma with bronchioloalveolar carcinoma features</atitle><jtitle>European journal of cardio-thoracic surgery</jtitle><addtitle>Eur J Cardiothorac Surg</addtitle><date>2013-04</date><risdate>2013</risdate><volume>43</volume><issue>4</issue><spage>765</spage><epage>771</epage><pages>765-771</pages><issn>1010-7940</issn><eissn>1873-734X</eissn><abstract>OBJECTIVES Pure bronchioloalveolar carcinoma (BAC) is considered the early stage of lung adenocarcinoma, and is even regarded as lung adenocarcinoma in situ. This study was designed to investigate the differences in the gene expression of pure BAC and that of adenocarcinoma with bronchioloalveolar features and explore the mechanism of BAC progression to adenocarcinoma with bronchioloalveolar features METHODS Total RNA was extracted from 16 tissue specimens. Expression analysis was carried out using Agilent 4 × 44 k arrays. Gene ontology analysis was used to define pathways altered in bronchioloalveolar progression. Differentially expressed candidate genes were validated using quantitative real-time PCR. The statistical analysis was carried out according to the methods of the paired t-test. RESULTS Adenocarcinoma with bronchioloalveolar features demonstrated an increased expression of 23 genes and reduced expression of 20 genes compared with BAC. These genes were considered candidate marker genes for tumour progression and metastasis. Genes overexpressed in adenocarcinoma with bronchioloalveolar features included fibroblast growth factor receptor 1, and CLDN18 (claudin 18), whereas those overexpressed in BAC included ataxia telangiectasia and Rad3 related (ataxia telangiectasia mutated and Rad3-related), and activating transcription factor 2. Mitogen-activated protein kinase (MAPK) pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with pure BAC. CONCLUSIONS Microarray-based expression profiling revealed interesting novel candidate genes in BAC and adenocarcinoma with bronchioloalveolar features. The MAPK pathway seemed dysregulated in adenocarcinoma with bronchioloalveolar features compared with the pure BAC pathway, which is worthy of being explored because it could partially explain the mechanism of the progression of BAC to adenocarcinoma with bronchioloalveolar features.</abstract><cop>Germany</cop><pub>Oxford University Press</pub><pmid>22864788</pmid><doi>10.1093/ejcts/ezs427</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adenocarcinoma - chemistry
Adenocarcinoma - classification
Adenocarcinoma - diagnosis
Adenocarcinoma - metabolism
Adenocarcinoma of Lung
Adenocarcinoma, Bronchiolo-Alveolar - classification
Adenocarcinoma, Bronchiolo-Alveolar - diagnosis
Adenocarcinoma, Bronchiolo-Alveolar - genetics
Adenocarcinoma, Bronchiolo-Alveolar - metabolism
Aged
Aged, 80 and over
Diagnosis, Differential
Female
Gene Expression Profiling
Humans
Lung Neoplasms - chemistry
Lung Neoplasms - classification
Lung Neoplasms - diagnosis
Lung Neoplasms - genetics
Lung Neoplasms - metabolism
Male
Middle Aged
Neoplasm Proteins - biosynthesis
Neoplasm Proteins - genetics
Neoplasm Staging
Oligonucleotide Array Sequence Analysis
Real-Time Polymerase Chain Reaction
RNA, Messenger - analysis
RNA, Messenger - metabolism
title Global gene expression differentiating pure bronchioloalveolar carcinoma from adenocarcinoma with bronchioloalveolar carcinoma features
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