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Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

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Rambau_et_al-2018-The_Journal_of_Pathology%3A_Clinical_Research.pdfAccepted version1.11 MBAdobe PDFView/Open
Title: Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study
Authors: Rambau, PF
Vierkant, RA
Intermaggio, MP
Kelemen, LE
Goodman, MT
Herpel, E
Pharoah, PD
Kommoss, S
Jimenez-Linan, M
Karlan, BY
Gentry-Maharaj, A
Menon, U
Hernando Polo, S
Candido Dos Reis, FJ
Doherty, JA
Gayther, SA
Sharma, R
Larson, MC
Harnett, PR
Hatfield, E
De Andrade, JM
Nelson, GS
Steed, H
Schildkraut, JM
Carney, ME
Høgdall, E
Whittemore, AS
Widschwendter, M
Kennedy, CJ
Wang, F
Wang, Q
Wang, C
Armasu, SM
Daley, F
Coulson, P
Jones, ME
Anglesio, MS
Chow, C
DeFazio, A
García-Closas, M
Brucker, SY
Cybulski, C
Harris, HR
Hartkopf, AD
Huzarski, T
Jensen, A
Lubiński, J
Oszurek, O
Benitez, J
Fady, M
Staebler, A
Taran, FA
Pasternak, J
Talhouk, A
Rossing, MA
Hendley, J
AOCS Group
Edwards, RP
Fereday, S
Modugno, F
Ness, RB
Sieh, W
El-Bahrawy, MA
Winham, SJ
Lester, J
Kjaer, SK
Gronwald, J
Sinn, P
Fasching, PA
Chang-Claude, J
Moysich, KB
Bowtell, DD
Hernandez, BY
Luk, H
Behrens, S
Shah, M
Jung, A
Ghatage, P
Alsop, J
Alsop, K
García-Donas, J
Thompson, PJ
Swerdlow, AJ
Karpinskyj, C
Cazorla-Jiménez, A
García, MJ
Deen, S
Wilkens, LR
Palacios, J
Berchuck, A
Koziak, JM
Brenton, JD
Cook, LS
Goode, EL
Huntsman, DG
Ramus, SJ
Köbel, M
Item Type: Journal Article
Abstract: We aimed to validate the prognostic association of p16 expression in ovarian high-grade serous carcinomas (HGSC) and to explore it in other ovarian carcinoma histotypes. p16 protein expression was assessed by clinical-grade immunohistochemistry in 6,525 ovarian carcinomas including 4,334 HGSC using tissue microarrays from 24 studies participating in the Ovarian Tumor Tissue Analysis (OTTA) consortium. p16 expression patterns were interpreted as abnormal (either overexpression referred to as block expression or absence) or normal (heterogeneous). CDKN2A (which encodes p16) mRNA expression was also analyzed in a subset (N=2,280) mostly representing HGSC (N=2,010). Association of p16 expression with overall survival (OS) was determined within histotypes as was CDKN2A expression for HGSC only. p16 block expression was most frequent in HGSC (56%) but neither protein nor mRNA expression was associated with OS. However, relative to heterogeneous expression, block expression was associated with shorter OS in endometriosis-associated carcinomas, clear cell (HR: 2.02, 95%CI 1.47-2.77, p< 0.001) and endometrioid (HR: 1.88, 95%CI 1.30- 2.75, p=0.004), while absence was associated with shorter OS in low-grade serous carcinomas (HR: 2.95, 95%CI 1.61-5.38, p=0.001). Absence was most frequent in mucinous carcinoma (50%), and was not associated with OS in this histotype. The prognostic value of p16 expression is histotype-specific and pattern dependent. We provide definitive evidence against an association of p16 expression with survival in ovarian HGSC as previously suggested. Block expression of p16 in clear cell and endometrioid carcinoma should be further validated as a prognostic marker, and absence in low-grade serous carcinoma justifies CDK4 inhibition. This article is protected by copyright. All rights reserved.
Issue Date: 1-Oct-2018
Date of Acceptance: 16-Jul-2018
URI: http://hdl.handle.net/10044/1/62316
DOI: https://dx.doi.org/10.1002/cjp2.109
ISSN: 2056-4538
Publisher: Wiley Open Access
Start Page: 250
End Page: 261
Journal / Book Title: Journal of Pathology: Clinical Research
Volume: 4
Issue: 4
Copyright Statement: © 2018 Wiley. This is the accepted version of the following article: . Accepted Author Manuscript, which has been published in final form at https://dx.doi.org/10.1002/cjp2.109. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Keywords: Science & Technology
Life Sciences & Biomedicine
Pathology
ovary
immunocytochemistry
RT-QPCR
GRADE SEROUS CARCINOMA
BRCA2 MUTATION CARRIERS
CANCER RISK
GROWTH-FACTOR
GENE-PRODUCT
SURVIVAL
P16(INK4A)
THERAPY
PATHWAY
PROTEIN
RT-QPCR
immunocytochemistry
ovary
AOCS Group
Immunocytochemistry
Ovary
RT-QPCR
Publication Status: Published
Conference Place: England
Online Publication Date: 2018-07-30
Appears in Collections:Department of Metabolism, Digestion and Reproduction