Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan)
Contrary to reports with conflicting results, progesterone is suspected to play an important role in the development of tumours in the women. A research work was conducted to assess the significance of PGR SNPs (progesterone receptor) polymorphisms in the progression of breast cancer in southern Pun...
Gespeichert in:
Veröffentlicht in: | Pure and applied biology 2022-03, Vol.11 (3), p.181-190 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 190 |
---|---|
container_issue | 3 |
container_start_page | 181 |
container_title | Pure and applied biology |
container_volume | 11 |
creator | Sadia, Sobia |
description | Contrary to reports with conflicting results, progesterone is suspected to play an important role in the development of tumours in the women. A research work was conducted to assess the significance of PGR SNPs (progesterone receptor) polymorphisms in the progression of breast cancer in southern Punjab (Pakistan). Because of the lack of detailed analysis of PGR gene variations in the Pakistani community, two variants PROGINS and +331G/A were selected. The Radiology and Oncology Department at Nishtar Medical College and Hospital in Multan, Pakistan, assisted researchers for enrolling 100 invasive breast cancer patients and one hundred and fifteen healthy controls. DNA was isolated using a non-organic method, and two SNPs were analysed by (Polymerase Chain Reaction Restriction Fragment length polymorphism) PCR-RFLP. Study participants were examined for their clinical/family history, demographic factors (e.g. age, Menopause, age of menopause, marital status, gestation status, history of memory carcinoma, cigarette consumption, and chemical exposure), and other variables being related to specific symptomatology. The wild type allele of both SNPs was observed with highest prevalence in patients and control individuals followed by heterozygous allele while homozygous mutant allele was present in least numbers. Chi square statistics for PROGINS showed (p= 0.448) an evidence of non-significant association while +331G/A variant (p=0.004) showed an inverse association with breast cancer risk. Further genetic studies using progesterone receptors for breast cancer risk can use our results as a database. |
doi_str_mv | 10.19045/bspab.2022.110020 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2615437150</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2615437150</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1640-bc092f464f9d56cedb21e3bd7ac7db5b085f7a2af2bfe6141a94112fa403fb3</originalsourceid><addsrcrecordid>eNpNkFFLwzAQx4MoOOa-gE8BX_Sh85Km7erbGE6FgYP5HpI0YZ1t0-Vaod_ebvPBe7mD_-8O7kfIPYM5y0EkzxpbpeccOJ8zBsDhikx4DCLiIltc_5tvyQzxAGPlWQxZMiHHZaOqAUuk3tGtoMEa23Y-IG19NdQ-tPsSa6RlQ7u9pYX9sZVva9t0pwUdrMKOGtUYG17okmLXF8Mp2fl-5ENDt31zUJo-btV3iZ1qnu7IjVMV2tlfn5Ld-vVr9R5tPt8-VstNZFgqINIGcu5EKlxeJKmxhebMxrrIlMkKnWhYJC5TXDmunU2ZYCoXjHGnBMROx1PycLnaBn_sLXby4Psw_oqSpywRccYSGCl-oUzwiME62YayVmGQDOTZrTy7lSe38uI2_gVNOm6g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2615437150</pqid></control><display><type>article</type><title>Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan)</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>Sadia, Sobia</creator><creatorcontrib>Sadia, Sobia</creatorcontrib><description>Contrary to reports with conflicting results, progesterone is suspected to play an important role in the development of tumours in the women. A research work was conducted to assess the significance of PGR SNPs (progesterone receptor) polymorphisms in the progression of breast cancer in southern Punjab (Pakistan). Because of the lack of detailed analysis of PGR gene variations in the Pakistani community, two variants PROGINS and +331G/A were selected. The Radiology and Oncology Department at Nishtar Medical College and Hospital in Multan, Pakistan, assisted researchers for enrolling 100 invasive breast cancer patients and one hundred and fifteen healthy controls. DNA was isolated using a non-organic method, and two SNPs were analysed by (Polymerase Chain Reaction Restriction Fragment length polymorphism) PCR-RFLP. Study participants were examined for their clinical/family history, demographic factors (e.g. age, Menopause, age of menopause, marital status, gestation status, history of memory carcinoma, cigarette consumption, and chemical exposure), and other variables being related to specific symptomatology. The wild type allele of both SNPs was observed with highest prevalence in patients and control individuals followed by heterozygous allele while homozygous mutant allele was present in least numbers. Chi square statistics for PROGINS showed (p= 0.448) an evidence of non-significant association while +331G/A variant (p=0.004) showed an inverse association with breast cancer risk. Further genetic studies using progesterone receptors for breast cancer risk can use our results as a database.</description><identifier>ISSN: 2304-2478</identifier><identifier>EISSN: 2304-2478</identifier><identifier>DOI: 10.19045/bspab.2022.110020</identifier><language>eng</language><publisher>Quetta: International Society of Pure and Applied Biology</publisher><subject>Age ; Alleles ; Breast cancer ; Chi-square test ; Estrogens ; Family medical history ; Genes ; Genetics ; Health care ; Health risks ; Invasiveness ; Medical research ; Menopause ; Ovaries ; Patients ; Polymerase chain reaction ; Polymorphism ; Progesterone ; Progesterone receptors ; Radiology ; Receptors ; Restriction fragment length polymorphism ; Risk factors ; Single-nucleotide polymorphism ; Smoking ; Statistical analysis ; Statistical tests ; Tumors ; Womens health</subject><ispartof>Pure and applied biology, 2022-03, Vol.11 (3), p.181-190</ispartof><rights>2022. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1640-bc092f464f9d56cedb21e3bd7ac7db5b085f7a2af2bfe6141a94112fa403fb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Sadia, Sobia</creatorcontrib><title>Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan)</title><title>Pure and applied biology</title><description>Contrary to reports with conflicting results, progesterone is suspected to play an important role in the development of tumours in the women. A research work was conducted to assess the significance of PGR SNPs (progesterone receptor) polymorphisms in the progression of breast cancer in southern Punjab (Pakistan). Because of the lack of detailed analysis of PGR gene variations in the Pakistani community, two variants PROGINS and +331G/A were selected. The Radiology and Oncology Department at Nishtar Medical College and Hospital in Multan, Pakistan, assisted researchers for enrolling 100 invasive breast cancer patients and one hundred and fifteen healthy controls. DNA was isolated using a non-organic method, and two SNPs were analysed by (Polymerase Chain Reaction Restriction Fragment length polymorphism) PCR-RFLP. Study participants were examined for their clinical/family history, demographic factors (e.g. age, Menopause, age of menopause, marital status, gestation status, history of memory carcinoma, cigarette consumption, and chemical exposure), and other variables being related to specific symptomatology. The wild type allele of both SNPs was observed with highest prevalence in patients and control individuals followed by heterozygous allele while homozygous mutant allele was present in least numbers. Chi square statistics for PROGINS showed (p= 0.448) an evidence of non-significant association while +331G/A variant (p=0.004) showed an inverse association with breast cancer risk. Further genetic studies using progesterone receptors for breast cancer risk can use our results as a database.</description><subject>Age</subject><subject>Alleles</subject><subject>Breast cancer</subject><subject>Chi-square test</subject><subject>Estrogens</subject><subject>Family medical history</subject><subject>Genes</subject><subject>Genetics</subject><subject>Health care</subject><subject>Health risks</subject><subject>Invasiveness</subject><subject>Medical research</subject><subject>Menopause</subject><subject>Ovaries</subject><subject>Patients</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism</subject><subject>Progesterone</subject><subject>Progesterone receptors</subject><subject>Radiology</subject><subject>Receptors</subject><subject>Restriction fragment length polymorphism</subject><subject>Risk factors</subject><subject>Single-nucleotide polymorphism</subject><subject>Smoking</subject><subject>Statistical analysis</subject><subject>Statistical tests</subject><subject>Tumors</subject><subject>Womens health</subject><issn>2304-2478</issn><issn>2304-2478</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpNkFFLwzAQx4MoOOa-gE8BX_Sh85Km7erbGE6FgYP5HpI0YZ1t0-Vaod_ebvPBe7mD_-8O7kfIPYM5y0EkzxpbpeccOJ8zBsDhikx4DCLiIltc_5tvyQzxAGPlWQxZMiHHZaOqAUuk3tGtoMEa23Y-IG19NdQ-tPsSa6RlQ7u9pYX9sZVva9t0pwUdrMKOGtUYG17okmLXF8Mp2fl-5ENDt31zUJo-btV3iZ1qnu7IjVMV2tlfn5Ld-vVr9R5tPt8-VstNZFgqINIGcu5EKlxeJKmxhebMxrrIlMkKnWhYJC5TXDmunU2ZYCoXjHGnBMROx1PycLnaBn_sLXby4Psw_oqSpywRccYSGCl-oUzwiME62YayVmGQDOTZrTy7lSe38uI2_gVNOm6g</recordid><startdate>20220310</startdate><enddate>20220310</enddate><creator>Sadia, Sobia</creator><general>International Society of Pure and Applied Biology</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20220310</creationdate><title>Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan)</title><author>Sadia, Sobia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1640-bc092f464f9d56cedb21e3bd7ac7db5b085f7a2af2bfe6141a94112fa403fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Age</topic><topic>Alleles</topic><topic>Breast cancer</topic><topic>Chi-square test</topic><topic>Estrogens</topic><topic>Family medical history</topic><topic>Genes</topic><topic>Genetics</topic><topic>Health care</topic><topic>Health risks</topic><topic>Invasiveness</topic><topic>Medical research</topic><topic>Menopause</topic><topic>Ovaries</topic><topic>Patients</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism</topic><topic>Progesterone</topic><topic>Progesterone receptors</topic><topic>Radiology</topic><topic>Receptors</topic><topic>Restriction fragment length polymorphism</topic><topic>Risk factors</topic><topic>Single-nucleotide polymorphism</topic><topic>Smoking</topic><topic>Statistical analysis</topic><topic>Statistical tests</topic><topic>Tumors</topic><topic>Womens health</topic><toplevel>online_resources</toplevel><creatorcontrib>Sadia, Sobia</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content 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 Basic</collection><jtitle>Pure and applied biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sadia, Sobia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan)</atitle><jtitle>Pure and applied biology</jtitle><date>2022-03-10</date><risdate>2022</risdate><volume>11</volume><issue>3</issue><spage>181</spage><epage>190</epage><pages>181-190</pages><issn>2304-2478</issn><eissn>2304-2478</eissn><abstract>Contrary to reports with conflicting results, progesterone is suspected to play an important role in the development of tumours in the women. A research work was conducted to assess the significance of PGR SNPs (progesterone receptor) polymorphisms in the progression of breast cancer in southern Punjab (Pakistan). Because of the lack of detailed analysis of PGR gene variations in the Pakistani community, two variants PROGINS and +331G/A were selected. The Radiology and Oncology Department at Nishtar Medical College and Hospital in Multan, Pakistan, assisted researchers for enrolling 100 invasive breast cancer patients and one hundred and fifteen healthy controls. DNA was isolated using a non-organic method, and two SNPs were analysed by (Polymerase Chain Reaction Restriction Fragment length polymorphism) PCR-RFLP. Study participants were examined for their clinical/family history, demographic factors (e.g. age, Menopause, age of menopause, marital status, gestation status, history of memory carcinoma, cigarette consumption, and chemical exposure), and other variables being related to specific symptomatology. The wild type allele of both SNPs was observed with highest prevalence in patients and control individuals followed by heterozygous allele while homozygous mutant allele was present in least numbers. Chi square statistics for PROGINS showed (p= 0.448) an evidence of non-significant association while +331G/A variant (p=0.004) showed an inverse association with breast cancer risk. Further genetic studies using progesterone receptors for breast cancer risk can use our results as a database.</abstract><cop>Quetta</cop><pub>International Society of Pure and Applied Biology</pub><doi>10.19045/bspab.2022.110020</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2304-2478 |
ispartof | Pure and applied biology, 2022-03, Vol.11 (3), p.181-190 |
issn | 2304-2478 2304-2478 |
language | eng |
recordid | cdi_proquest_journals_2615437150 |
source | EZB-FREE-00999 freely available EZB journals |
subjects | Age Alleles Breast cancer Chi-square test Estrogens Family medical history Genes Genetics Health care Health risks Invasiveness Medical research Menopause Ovaries Patients Polymerase chain reaction Polymorphism Progesterone Progesterone receptors Radiology Receptors Restriction fragment length polymorphism Risk factors Single-nucleotide polymorphism Smoking Statistical analysis Statistical tests Tumors Womens health |
title | Analysis of P4 receptors polymorphisms in the development of breast cancer: A study of Southern Punjab (Pakistan) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T15%3A56%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Analysis%20of%20P4%20receptors%20polymorphisms%20in%20the%20development%20of%20breast%20cancer:%20A%20study%20of%20Southern%20Punjab%20(Pakistan)&rft.jtitle=Pure%20and%20applied%20biology&rft.au=Sadia,%20Sobia&rft.date=2022-03-10&rft.volume=11&rft.issue=3&rft.spage=181&rft.epage=190&rft.pages=181-190&rft.issn=2304-2478&rft.eissn=2304-2478&rft_id=info:doi/10.19045/bspab.2022.110020&rft_dat=%3Cproquest_cross%3E2615437150%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2615437150&rft_id=info:pmid/&rfr_iscdi=true |