Loading…
Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients
Pancreatic cancer has a poor prognosis; hence, novel prognostic markers and effective therapeutic targets should be identified. We aimed to evaluate folate receptor alpha (FR-α) expression in pancreatic cancer and examine its association with clinicopathological features. We utilized tissue samples...
Saved in:
Published in: | Medical molecular morphology 2018-12, Vol.51 (4), p.237-243 |
---|---|
Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373 |
---|---|
cites | cdi_FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373 |
container_end_page | 243 |
container_issue | 4 |
container_start_page | 237 |
container_title | Medical molecular morphology |
container_volume | 51 |
creator | Omote, Shizuma Takata, Katsuyoshi Tanaka, Takehiro Miyata-Takata, Tomoko Ayada, Yoshiyuki Noujima-Harada, Mai Omote, Rika Tabata, Tetsuya Sato, Yasuharu Toyokawa, Tatsuya Kato, Hironari Yagi, Takahito Okada, Hiroyuki Yoshino, Tadashi |
description | Pancreatic cancer has a poor prognosis; hence, novel prognostic markers and effective therapeutic targets should be identified. We aimed to evaluate folate receptor alpha (FR-α) expression in pancreatic cancer and examine its association with clinicopathological features. We utilized tissue samples from 100 primary pancreatic cancer patients who underwent surgery. FR-α was expressed in 37 of 100 cases (37%). The FR-α-positive group (median, 18.8 months) had a significantly poorer prognosis than the FR-α-negative group [median 21.3 months; HR 1.89 (1.12–3.12);
P
= 0.017]. These groups were not significantly different regarding progression-free survival (
P
= 0.196). Furthermore, other serum tumor markers including CA19-9 (mean, 186 vs. 822 U/ml;
P
= 0.001), Dupan-2 (286 vs. 1133 U/ml;
P
= 0.000), and Span-1 (69.7 vs. 171.9 U/ml;
P
= 0.006) were significantly downregulated in the FR-α-positive group. CA19-9 was another prognostic factor, in addition to FR-α, and patient prognosis showed clear stratification curves with the expression of these two molecules. Along with CA19-9, FR-α expression was an independent prognostic factor for the overall survival. FR-α and CA19-9 helped predict patient prognosis based on stratification curves. |
doi_str_mv | 10.1007/s00795-018-0197-8 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2057870664</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2057870664</sourcerecordid><originalsourceid>FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373</originalsourceid><addsrcrecordid>eNp1kUlLBDEQhYMojtsP8CIBL15as0w6yVHEDQQveg6ZdEVbepI26R7035t2XEDwUJUi-d5LwUPokJJTSog8y6VpURGqSmlZqQ20Q1VNKjrXevNnVmSGdnN-IYTLmoltNGNas5pqsoNW9ytI8NYnyLmNAUePfezsADiBg36ICduuf7a4zdgG3IYGeigtDLhP8SnEPLQOe-sm0peK4-DiEvLk1NvgEtiJcGWEVG6GtmjzPtrytstw8HXuocery4eLm-ru_vr24vyucoLxofIMlOCSKClEIyWxjHCx0A1VjEteO94w7vVcWacWys-JbESjKGdMcSloQfbQydq3LPs6Qh7Mss0Ous4GiGM2jAipJKnreUGP_6AvcUyhbPdJsYKwyZCuKZdizgm86VO7tOndUGKmUMw6FFNCMVMoRhXN0ZfzuFhC86P4TqEAbA3k8hSeIP1-_b_rBysbl00</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2057264327</pqid></control><display><type>article</type><title>Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients</title><source>Springer Nature</source><creator>Omote, Shizuma ; Takata, Katsuyoshi ; Tanaka, Takehiro ; Miyata-Takata, Tomoko ; Ayada, Yoshiyuki ; Noujima-Harada, Mai ; Omote, Rika ; Tabata, Tetsuya ; Sato, Yasuharu ; Toyokawa, Tatsuya ; Kato, Hironari ; Yagi, Takahito ; Okada, Hiroyuki ; Yoshino, Tadashi</creator><creatorcontrib>Omote, Shizuma ; Takata, Katsuyoshi ; Tanaka, Takehiro ; Miyata-Takata, Tomoko ; Ayada, Yoshiyuki ; Noujima-Harada, Mai ; Omote, Rika ; Tabata, Tetsuya ; Sato, Yasuharu ; Toyokawa, Tatsuya ; Kato, Hironari ; Yagi, Takahito ; Okada, Hiroyuki ; Yoshino, Tadashi</creatorcontrib><description>Pancreatic cancer has a poor prognosis; hence, novel prognostic markers and effective therapeutic targets should be identified. We aimed to evaluate folate receptor alpha (FR-α) expression in pancreatic cancer and examine its association with clinicopathological features. We utilized tissue samples from 100 primary pancreatic cancer patients who underwent surgery. FR-α was expressed in 37 of 100 cases (37%). The FR-α-positive group (median, 18.8 months) had a significantly poorer prognosis than the FR-α-negative group [median 21.3 months; HR 1.89 (1.12–3.12);
P
= 0.017]. These groups were not significantly different regarding progression-free survival (
P
= 0.196). Furthermore, other serum tumor markers including CA19-9 (mean, 186 vs. 822 U/ml;
P
= 0.001), Dupan-2 (286 vs. 1133 U/ml;
P
= 0.000), and Span-1 (69.7 vs. 171.9 U/ml;
P
= 0.006) were significantly downregulated in the FR-α-positive group. CA19-9 was another prognostic factor, in addition to FR-α, and patient prognosis showed clear stratification curves with the expression of these two molecules. Along with CA19-9, FR-α expression was an independent prognostic factor for the overall survival. FR-α and CA19-9 helped predict patient prognosis based on stratification curves.</description><identifier>ISSN: 1860-1480</identifier><identifier>EISSN: 1860-1499</identifier><identifier>DOI: 10.1007/s00795-018-0197-8</identifier><identifier>PMID: 29926190</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Anatomy ; Folic acid ; Medical prognosis ; Medicine ; Medicine & Public Health ; Molecular Medicine ; Original Paper ; Pancreatic cancer ; Pathology ; Prognosis ; Surgery ; Survival ; Therapeutic applications ; Tumor markers</subject><ispartof>Medical molecular morphology, 2018-12, Vol.51 (4), p.237-243</ispartof><rights>The Japanese Society for Clinical Molecular Morphology 2018</rights><rights>Medical Molecular Morphology is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373</citedby><cites>FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373</cites><orcidid>0000-0002-0557-9125</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29926190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Omote, Shizuma</creatorcontrib><creatorcontrib>Takata, Katsuyoshi</creatorcontrib><creatorcontrib>Tanaka, Takehiro</creatorcontrib><creatorcontrib>Miyata-Takata, Tomoko</creatorcontrib><creatorcontrib>Ayada, Yoshiyuki</creatorcontrib><creatorcontrib>Noujima-Harada, Mai</creatorcontrib><creatorcontrib>Omote, Rika</creatorcontrib><creatorcontrib>Tabata, Tetsuya</creatorcontrib><creatorcontrib>Sato, Yasuharu</creatorcontrib><creatorcontrib>Toyokawa, Tatsuya</creatorcontrib><creatorcontrib>Kato, Hironari</creatorcontrib><creatorcontrib>Yagi, Takahito</creatorcontrib><creatorcontrib>Okada, Hiroyuki</creatorcontrib><creatorcontrib>Yoshino, Tadashi</creatorcontrib><title>Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients</title><title>Medical molecular morphology</title><addtitle>Med Mol Morphol</addtitle><addtitle>Med Mol Morphol</addtitle><description>Pancreatic cancer has a poor prognosis; hence, novel prognostic markers and effective therapeutic targets should be identified. We aimed to evaluate folate receptor alpha (FR-α) expression in pancreatic cancer and examine its association with clinicopathological features. We utilized tissue samples from 100 primary pancreatic cancer patients who underwent surgery. FR-α was expressed in 37 of 100 cases (37%). The FR-α-positive group (median, 18.8 months) had a significantly poorer prognosis than the FR-α-negative group [median 21.3 months; HR 1.89 (1.12–3.12);
P
= 0.017]. These groups were not significantly different regarding progression-free survival (
P
= 0.196). Furthermore, other serum tumor markers including CA19-9 (mean, 186 vs. 822 U/ml;
P
= 0.001), Dupan-2 (286 vs. 1133 U/ml;
P
= 0.000), and Span-1 (69.7 vs. 171.9 U/ml;
P
= 0.006) were significantly downregulated in the FR-α-positive group. CA19-9 was another prognostic factor, in addition to FR-α, and patient prognosis showed clear stratification curves with the expression of these two molecules. Along with CA19-9, FR-α expression was an independent prognostic factor for the overall survival. FR-α and CA19-9 helped predict patient prognosis based on stratification curves.</description><subject>Anatomy</subject><subject>Folic acid</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Molecular Medicine</subject><subject>Original Paper</subject><subject>Pancreatic cancer</subject><subject>Pathology</subject><subject>Prognosis</subject><subject>Surgery</subject><subject>Survival</subject><subject>Therapeutic applications</subject><subject>Tumor markers</subject><issn>1860-1480</issn><issn>1860-1499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kUlLBDEQhYMojtsP8CIBL15as0w6yVHEDQQveg6ZdEVbepI26R7035t2XEDwUJUi-d5LwUPokJJTSog8y6VpURGqSmlZqQ20Q1VNKjrXevNnVmSGdnN-IYTLmoltNGNas5pqsoNW9ytI8NYnyLmNAUePfezsADiBg36ICduuf7a4zdgG3IYGeigtDLhP8SnEPLQOe-sm0peK4-DiEvLk1NvgEtiJcGWEVG6GtmjzPtrytstw8HXuocery4eLm-ru_vr24vyucoLxofIMlOCSKClEIyWxjHCx0A1VjEteO94w7vVcWacWys-JbESjKGdMcSloQfbQydq3LPs6Qh7Mss0Ous4GiGM2jAipJKnreUGP_6AvcUyhbPdJsYKwyZCuKZdizgm86VO7tOndUGKmUMw6FFNCMVMoRhXN0ZfzuFhC86P4TqEAbA3k8hSeIP1-_b_rBysbl00</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Omote, Shizuma</creator><creator>Takata, Katsuyoshi</creator><creator>Tanaka, Takehiro</creator><creator>Miyata-Takata, Tomoko</creator><creator>Ayada, Yoshiyuki</creator><creator>Noujima-Harada, Mai</creator><creator>Omote, Rika</creator><creator>Tabata, Tetsuya</creator><creator>Sato, Yasuharu</creator><creator>Toyokawa, Tatsuya</creator><creator>Kato, Hironari</creator><creator>Yagi, Takahito</creator><creator>Okada, Hiroyuki</creator><creator>Yoshino, Tadashi</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</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>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>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0557-9125</orcidid></search><sort><creationdate>20181201</creationdate><title>Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients</title><author>Omote, Shizuma ; Takata, Katsuyoshi ; Tanaka, Takehiro ; Miyata-Takata, Tomoko ; Ayada, Yoshiyuki ; Noujima-Harada, Mai ; Omote, Rika ; Tabata, Tetsuya ; Sato, Yasuharu ; Toyokawa, Tatsuya ; Kato, Hironari ; Yagi, Takahito ; Okada, Hiroyuki ; Yoshino, Tadashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anatomy</topic><topic>Folic acid</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Molecular Medicine</topic><topic>Original Paper</topic><topic>Pancreatic cancer</topic><topic>Pathology</topic><topic>Prognosis</topic><topic>Surgery</topic><topic>Survival</topic><topic>Therapeutic applications</topic><topic>Tumor markers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Omote, Shizuma</creatorcontrib><creatorcontrib>Takata, Katsuyoshi</creatorcontrib><creatorcontrib>Tanaka, Takehiro</creatorcontrib><creatorcontrib>Miyata-Takata, Tomoko</creatorcontrib><creatorcontrib>Ayada, Yoshiyuki</creatorcontrib><creatorcontrib>Noujima-Harada, Mai</creatorcontrib><creatorcontrib>Omote, Rika</creatorcontrib><creatorcontrib>Tabata, Tetsuya</creatorcontrib><creatorcontrib>Sato, Yasuharu</creatorcontrib><creatorcontrib>Toyokawa, Tatsuya</creatorcontrib><creatorcontrib>Kato, Hironari</creatorcontrib><creatorcontrib>Yagi, Takahito</creatorcontrib><creatorcontrib>Okada, Hiroyuki</creatorcontrib><creatorcontrib>Yoshino, Tadashi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</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>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Nursing & Allied Health Premium</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>Medical molecular morphology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Omote, Shizuma</au><au>Takata, Katsuyoshi</au><au>Tanaka, Takehiro</au><au>Miyata-Takata, Tomoko</au><au>Ayada, Yoshiyuki</au><au>Noujima-Harada, Mai</au><au>Omote, Rika</au><au>Tabata, Tetsuya</au><au>Sato, Yasuharu</au><au>Toyokawa, Tatsuya</au><au>Kato, Hironari</au><au>Yagi, Takahito</au><au>Okada, Hiroyuki</au><au>Yoshino, Tadashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients</atitle><jtitle>Medical molecular morphology</jtitle><stitle>Med Mol Morphol</stitle><addtitle>Med Mol Morphol</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>51</volume><issue>4</issue><spage>237</spage><epage>243</epage><pages>237-243</pages><issn>1860-1480</issn><eissn>1860-1499</eissn><abstract>Pancreatic cancer has a poor prognosis; hence, novel prognostic markers and effective therapeutic targets should be identified. We aimed to evaluate folate receptor alpha (FR-α) expression in pancreatic cancer and examine its association with clinicopathological features. We utilized tissue samples from 100 primary pancreatic cancer patients who underwent surgery. FR-α was expressed in 37 of 100 cases (37%). The FR-α-positive group (median, 18.8 months) had a significantly poorer prognosis than the FR-α-negative group [median 21.3 months; HR 1.89 (1.12–3.12);
P
= 0.017]. These groups were not significantly different regarding progression-free survival (
P
= 0.196). Furthermore, other serum tumor markers including CA19-9 (mean, 186 vs. 822 U/ml;
P
= 0.001), Dupan-2 (286 vs. 1133 U/ml;
P
= 0.000), and Span-1 (69.7 vs. 171.9 U/ml;
P
= 0.006) were significantly downregulated in the FR-α-positive group. CA19-9 was another prognostic factor, in addition to FR-α, and patient prognosis showed clear stratification curves with the expression of these two molecules. Along with CA19-9, FR-α expression was an independent prognostic factor for the overall survival. FR-α and CA19-9 helped predict patient prognosis based on stratification curves.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>29926190</pmid><doi>10.1007/s00795-018-0197-8</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0557-9125</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1860-1480 |
ispartof | Medical molecular morphology, 2018-12, Vol.51 (4), p.237-243 |
issn | 1860-1480 1860-1499 |
language | eng |
recordid | cdi_proquest_miscellaneous_2057870664 |
source | Springer Nature |
subjects | Anatomy Folic acid Medical prognosis Medicine Medicine & Public Health Molecular Medicine Original Paper Pancreatic cancer Pathology Prognosis Surgery Survival Therapeutic applications Tumor markers |
title | Overexpression of folate receptor alpha is an independent prognostic factor for outcomes of pancreatic cancer patients |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T09%3A25%3A05IST&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=Overexpression%20of%20folate%20receptor%20alpha%20is%20an%20independent%20prognostic%20factor%20for%20outcomes%20of%20pancreatic%20cancer%20patients&rft.jtitle=Medical%20molecular%20morphology&rft.au=Omote,%20Shizuma&rft.date=2018-12-01&rft.volume=51&rft.issue=4&rft.spage=237&rft.epage=243&rft.pages=237-243&rft.issn=1860-1480&rft.eissn=1860-1499&rft_id=info:doi/10.1007/s00795-018-0197-8&rft_dat=%3Cproquest_cross%3E2057870664%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2057264327&rft_id=info:pmid/29926190&rfr_iscdi=true |