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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...

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Published in:Medical molecular morphology 2018-12, Vol.51 (4), p.237-243
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c523t-f2e853708755d770a2035b9d1823736c3d23f948ac8b8f407d5d8132283751373
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container_title Medical molecular morphology
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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
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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. 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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
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