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Detection of differential expression of miRNAs in computerized tomography-guided lung biopsy
Aims: Nonsmall-cell lung carcinoma comprises 85% of lung malignancies and is usually associated with a poor prognosis due to diagnosis at advanced stages. Molecular diagnosis of computerized tomography (CT)-guided biopsy has the potential to identify subtypes of lung carcinoma like adenocarcinoma (A...
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Published in: | Journal of cancer research and therapeutics 2022-01, Vol.18 (1), p.231-239 |
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creator | Singh, Anjana Kant, Ravi Nandi, Soumyadeep Husain, Nuzhat Naithani, Manisha Mirza, Anissa Saluja, Tajindra Srivastava, Kamini Prakash, Ved Singh, Satyendra |
description | Aims: Nonsmall-cell lung carcinoma comprises 85% of lung malignancies and is usually associated with a poor prognosis due to diagnosis at advanced stages. Molecular diagnosis of computerized tomography (CT)-guided biopsy has the potential to identify subtypes of lung carcinoma like adenocarcinoma (AC) and squamous cell carcinoma (SCC) along with its molecular stratification. This approach will help predict the genetic signature of lung cancer in individual patients.
Subjects and Methods: Histopathologically proved a CT-guided biopsy sample of lung cancer cases was used to screen for the expression of microRNA (miRNA) earlier quantitated in blood plasma. Primers against hsa-miR2114, hsa-miR2115, hsa-miR2116, hsa-miR2117, hsa-miR449c, and hsa-miR548q with control RNU6 were used to screen 30 AC, 30 SCC, 5 nonspecific granulomatous inflammation, and 8 control samples. Reverse transcription polymerase chain reaction (RT-PCR) data revealed expression of hsa-miR2114 and hsa-miR548q in AC as well as SCC.
Results: RT-PCR data revealed that the expression of hsa-miR2116 and hsa-miR449c was found upregulated in AC while hsa-miR2117 was expressed in SCC cases. Bioinformatic analysis revealed that genes, where these miRNAs are located, were also upregulated while targets of these miRNAs were downregulated.
Conclusions: miRNAs expression pattern in the CT-guided biopsy samples can be used as a potential tool to differentially diagnose lung cancer subtypes. The expression pattern of miRNAs matches very well in blood plasma and tissue samples, albeit levels were very low in the earlier case than later. This approach can also be used for screening mutations and other molecular markers in a personalized manner for the management of lung cancer patients. |
doi_str_mv | 10.4103/jcrt.jcrt_749_21 |
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fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2647654555</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A699360708</galeid><sourcerecordid>A699360708</sourcerecordid><originalsourceid>FETCH-LOGICAL-c463o-4c3dcd341cb892d9c0843e38b527c57cc663467d319c595c8fb78219e76b0ea83</originalsourceid><addsrcrecordid>eNp1kt2L1DAUxYMo7uzqu09S8MWXjknz_TjuuiosCqJvQmjT25rZNqlJyzj-9bbOrKwyEkjg5ndOPs5F6BnBa0YwfbW1cVwvk5FMm4I8QCuitcoZoeohWmEtaU6YKs7QeUpbjLksCvUYnVFOFZFKr9DXKxjBji74LDRZ7ZoGIvjRlV0GP4YIKR23evfpwyZlzmc29MM0QnQ_oc7G0Ic2lsO3fd5Orp4r3eTbrHJhSPsn6FFTdgmeHtcL9OX6zefLd_nNx7fvLzc3uWWChpxZWtuaMmIrpYtaW6wYBaoqXkjLpbVCUCZkTYm2XHOrmkqqgmiQosJQKnqBXh58hxi-T5BG07tkoetKD2FKphBMCs445zP64h90G6bo59stlCDLb92j2rID43wTxljaxdRshNZUYImXY_MTVAseYtkFD42by3_x6xP8PGronT0pwAeBjSGlCI0ZouvLuDcEm6UBzO_s7zXALHl-fN9U9VD_EdwlPgOvD8AudHOI6babdhDNzN76sPuvsSkoMXe9Qn8BtIjEUw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2646114825</pqid></control><display><type>article</type><title>Detection of differential expression of miRNAs in computerized tomography-guided lung biopsy</title><source>Publicly Available Content (ProQuest)</source><creator>Singh, Anjana ; Kant, Ravi ; Nandi, Soumyadeep ; Husain, Nuzhat ; Naithani, Manisha ; Mirza, Anissa ; Saluja, Tajindra ; Srivastava, Kamini ; Prakash, Ved ; Singh, Satyendra</creator><creatorcontrib>Singh, Anjana ; Kant, Ravi ; Nandi, Soumyadeep ; Husain, Nuzhat ; Naithani, Manisha ; Mirza, Anissa ; Saluja, Tajindra ; Srivastava, Kamini ; Prakash, Ved ; Singh, Satyendra</creatorcontrib><description>Aims: Nonsmall-cell lung carcinoma comprises 85% of lung malignancies and is usually associated with a poor prognosis due to diagnosis at advanced stages. Molecular diagnosis of computerized tomography (CT)-guided biopsy has the potential to identify subtypes of lung carcinoma like adenocarcinoma (AC) and squamous cell carcinoma (SCC) along with its molecular stratification. This approach will help predict the genetic signature of lung cancer in individual patients.
Subjects and Methods: Histopathologically proved a CT-guided biopsy sample of lung cancer cases was used to screen for the expression of microRNA (miRNA) earlier quantitated in blood plasma. Primers against hsa-miR2114, hsa-miR2115, hsa-miR2116, hsa-miR2117, hsa-miR449c, and hsa-miR548q with control RNU6 were used to screen 30 AC, 30 SCC, 5 nonspecific granulomatous inflammation, and 8 control samples. Reverse transcription polymerase chain reaction (RT-PCR) data revealed expression of hsa-miR2114 and hsa-miR548q in AC as well as SCC.
Results: RT-PCR data revealed that the expression of hsa-miR2116 and hsa-miR449c was found upregulated in AC while hsa-miR2117 was expressed in SCC cases. Bioinformatic analysis revealed that genes, where these miRNAs are located, were also upregulated while targets of these miRNAs were downregulated.
Conclusions: miRNAs expression pattern in the CT-guided biopsy samples can be used as a potential tool to differentially diagnose lung cancer subtypes. The expression pattern of miRNAs matches very well in blood plasma and tissue samples, albeit levels were very low in the earlier case than later. This approach can also be used for screening mutations and other molecular markers in a personalized manner for the management of lung cancer patients.</description><identifier>ISSN: 0973-1482</identifier><identifier>EISSN: 1998-4138</identifier><identifier>DOI: 10.4103/jcrt.jcrt_749_21</identifier><identifier>PMID: 35381789</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. Ltd</publisher><subject>Biopsy ; Cancer ; CT imaging ; Diagnosis ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genetic aspects ; Health aspects ; Humans ; Lung - diagnostic imaging ; Lung cancer ; Lung cancer, Non-small cell ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - genetics ; Lungs ; Methods ; MicroRNA ; MicroRNAs ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Molecular diagnostic techniques ; Oncology, Experimental ; Squamous cell carcinoma ; Tomography ; Tomography, X-Ray Computed</subject><ispartof>Journal of cancer research and therapeutics, 2022-01, Vol.18 (1), p.231-239</ispartof><rights>COPYRIGHT 2022 Medknow Publications and Media Pvt. Ltd.</rights><rights>2022. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463o-4c3dcd341cb892d9c0843e38b527c57cc663467d319c595c8fb78219e76b0ea83</citedby><cites>FETCH-LOGICAL-c463o-4c3dcd341cb892d9c0843e38b527c57cc663467d319c595c8fb78219e76b0ea83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2646114825?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35381789$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, Anjana</creatorcontrib><creatorcontrib>Kant, Ravi</creatorcontrib><creatorcontrib>Nandi, Soumyadeep</creatorcontrib><creatorcontrib>Husain, Nuzhat</creatorcontrib><creatorcontrib>Naithani, Manisha</creatorcontrib><creatorcontrib>Mirza, Anissa</creatorcontrib><creatorcontrib>Saluja, Tajindra</creatorcontrib><creatorcontrib>Srivastava, Kamini</creatorcontrib><creatorcontrib>Prakash, Ved</creatorcontrib><creatorcontrib>Singh, Satyendra</creatorcontrib><title>Detection of differential expression of miRNAs in computerized tomography-guided lung biopsy</title><title>Journal of cancer research and therapeutics</title><addtitle>J Cancer Res Ther</addtitle><description>Aims: Nonsmall-cell lung carcinoma comprises 85% of lung malignancies and is usually associated with a poor prognosis due to diagnosis at advanced stages. Molecular diagnosis of computerized tomography (CT)-guided biopsy has the potential to identify subtypes of lung carcinoma like adenocarcinoma (AC) and squamous cell carcinoma (SCC) along with its molecular stratification. This approach will help predict the genetic signature of lung cancer in individual patients.
Subjects and Methods: Histopathologically proved a CT-guided biopsy sample of lung cancer cases was used to screen for the expression of microRNA (miRNA) earlier quantitated in blood plasma. Primers against hsa-miR2114, hsa-miR2115, hsa-miR2116, hsa-miR2117, hsa-miR449c, and hsa-miR548q with control RNU6 were used to screen 30 AC, 30 SCC, 5 nonspecific granulomatous inflammation, and 8 control samples. Reverse transcription polymerase chain reaction (RT-PCR) data revealed expression of hsa-miR2114 and hsa-miR548q in AC as well as SCC.
Results: RT-PCR data revealed that the expression of hsa-miR2116 and hsa-miR449c was found upregulated in AC while hsa-miR2117 was expressed in SCC cases. Bioinformatic analysis revealed that genes, where these miRNAs are located, were also upregulated while targets of these miRNAs were downregulated.
Conclusions: miRNAs expression pattern in the CT-guided biopsy samples can be used as a potential tool to differentially diagnose lung cancer subtypes. The expression pattern of miRNAs matches very well in blood plasma and tissue samples, albeit levels were very low in the earlier case than later. This approach can also be used for screening mutations and other molecular markers in a personalized manner for the management of lung cancer patients.</description><subject>Biopsy</subject><subject>Cancer</subject><subject>CT imaging</subject><subject>Diagnosis</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lung - diagnostic imaging</subject><subject>Lung cancer</subject><subject>Lung cancer, Non-small cell</subject><subject>Lung Neoplasms - diagnostic imaging</subject><subject>Lung Neoplasms - genetics</subject><subject>Lungs</subject><subject>Methods</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Molecular diagnostic techniques</subject><subject>Oncology, Experimental</subject><subject>Squamous cell carcinoma</subject><subject>Tomography</subject><subject>Tomography, X-Ray Computed</subject><issn>0973-1482</issn><issn>1998-4138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1kt2L1DAUxYMo7uzqu09S8MWXjknz_TjuuiosCqJvQmjT25rZNqlJyzj-9bbOrKwyEkjg5ndOPs5F6BnBa0YwfbW1cVwvk5FMm4I8QCuitcoZoeohWmEtaU6YKs7QeUpbjLksCvUYnVFOFZFKr9DXKxjBji74LDRZ7ZoGIvjRlV0GP4YIKR23evfpwyZlzmc29MM0QnQ_oc7G0Ic2lsO3fd5Orp4r3eTbrHJhSPsn6FFTdgmeHtcL9OX6zefLd_nNx7fvLzc3uWWChpxZWtuaMmIrpYtaW6wYBaoqXkjLpbVCUCZkTYm2XHOrmkqqgmiQosJQKnqBXh58hxi-T5BG07tkoetKD2FKphBMCs445zP64h90G6bo59stlCDLb92j2rID43wTxljaxdRshNZUYImXY_MTVAseYtkFD42by3_x6xP8PGronT0pwAeBjSGlCI0ZouvLuDcEm6UBzO_s7zXALHl-fN9U9VD_EdwlPgOvD8AudHOI6babdhDNzN76sPuvsSkoMXe9Qn8BtIjEUw</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Singh, Anjana</creator><creator>Kant, Ravi</creator><creator>Nandi, Soumyadeep</creator><creator>Husain, Nuzhat</creator><creator>Naithani, Manisha</creator><creator>Mirza, Anissa</creator><creator>Saluja, Tajindra</creator><creator>Srivastava, Kamini</creator><creator>Prakash, Ved</creator><creator>Singh, Satyendra</creator><general>Wolters Kluwer India Pvt. 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Saluja, Tajindra ; Srivastava, Kamini ; Prakash, Ved ; Singh, Satyendra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463o-4c3dcd341cb892d9c0843e38b527c57cc663467d319c595c8fb78219e76b0ea83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biopsy</topic><topic>Cancer</topic><topic>CT imaging</topic><topic>Diagnosis</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Lung - diagnostic imaging</topic><topic>Lung cancer</topic><topic>Lung cancer, Non-small cell</topic><topic>Lung Neoplasms - diagnostic imaging</topic><topic>Lung Neoplasms - genetics</topic><topic>Lungs</topic><topic>Methods</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Molecular diagnostic techniques</topic><topic>Oncology, Experimental</topic><topic>Squamous cell carcinoma</topic><topic>Tomography</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Anjana</creatorcontrib><creatorcontrib>Kant, Ravi</creatorcontrib><creatorcontrib>Nandi, Soumyadeep</creatorcontrib><creatorcontrib>Husain, Nuzhat</creatorcontrib><creatorcontrib>Naithani, Manisha</creatorcontrib><creatorcontrib>Mirza, Anissa</creatorcontrib><creatorcontrib>Saluja, Tajindra</creatorcontrib><creatorcontrib>Srivastava, Kamini</creatorcontrib><creatorcontrib>Prakash, Ved</creatorcontrib><creatorcontrib>Singh, Satyendra</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>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cancer research and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Anjana</au><au>Kant, Ravi</au><au>Nandi, Soumyadeep</au><au>Husain, Nuzhat</au><au>Naithani, Manisha</au><au>Mirza, Anissa</au><au>Saluja, Tajindra</au><au>Srivastava, Kamini</au><au>Prakash, Ved</au><au>Singh, Satyendra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of differential expression of miRNAs in computerized tomography-guided lung biopsy</atitle><jtitle>Journal of cancer research and therapeutics</jtitle><addtitle>J Cancer Res Ther</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>18</volume><issue>1</issue><spage>231</spage><epage>239</epage><pages>231-239</pages><issn>0973-1482</issn><eissn>1998-4138</eissn><abstract>Aims: Nonsmall-cell lung carcinoma comprises 85% of lung malignancies and is usually associated with a poor prognosis due to diagnosis at advanced stages. Molecular diagnosis of computerized tomography (CT)-guided biopsy has the potential to identify subtypes of lung carcinoma like adenocarcinoma (AC) and squamous cell carcinoma (SCC) along with its molecular stratification. This approach will help predict the genetic signature of lung cancer in individual patients.
Subjects and Methods: Histopathologically proved a CT-guided biopsy sample of lung cancer cases was used to screen for the expression of microRNA (miRNA) earlier quantitated in blood plasma. Primers against hsa-miR2114, hsa-miR2115, hsa-miR2116, hsa-miR2117, hsa-miR449c, and hsa-miR548q with control RNU6 were used to screen 30 AC, 30 SCC, 5 nonspecific granulomatous inflammation, and 8 control samples. Reverse transcription polymerase chain reaction (RT-PCR) data revealed expression of hsa-miR2114 and hsa-miR548q in AC as well as SCC.
Results: RT-PCR data revealed that the expression of hsa-miR2116 and hsa-miR449c was found upregulated in AC while hsa-miR2117 was expressed in SCC cases. Bioinformatic analysis revealed that genes, where these miRNAs are located, were also upregulated while targets of these miRNAs were downregulated.
Conclusions: miRNAs expression pattern in the CT-guided biopsy samples can be used as a potential tool to differentially diagnose lung cancer subtypes. The expression pattern of miRNAs matches very well in blood plasma and tissue samples, albeit levels were very low in the earlier case than later. This approach can also be used for screening mutations and other molecular markers in a personalized manner for the management of lung cancer patients.</abstract><cop>India</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><pmid>35381789</pmid><doi>10.4103/jcrt.jcrt_749_21</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Cancer CT imaging Diagnosis Gene expression Gene Expression Profiling Gene Expression Regulation, Neoplastic Genetic aspects Health aspects Humans Lung - diagnostic imaging Lung cancer Lung cancer, Non-small cell Lung Neoplasms - diagnostic imaging Lung Neoplasms - genetics Lungs Methods MicroRNA MicroRNAs MicroRNAs - genetics MicroRNAs - metabolism Molecular diagnostic techniques Oncology, Experimental Squamous cell carcinoma Tomography Tomography, X-Ray Computed |
title | Detection of differential expression of miRNAs in computerized tomography-guided lung biopsy |
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