Analysis of MLH1 and MSH2 Expression in Ovarian Cancer before and after Platinum Drug-based Chemotherapy

Preclinical studies have demonstrated a relationship between DNA mismatch repair (MMR) status and sensitivity to cisplatin and carboplatin. MMR-deficient cells are resistant to both drugs, and selection for cisplatin resistance in vitro is sometimes accompanied by loss of MMR protein expression. We...

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Veröffentlicht in:Clinical cancer research 2000-04, Vol.6 (4), p.1415-1421
Hauptverfasser: SAMIMI, G, FINK, D, VARKI, N. M, HUSAIN, A, HOSKINS, W. J, ALBERTS, D. S, HOWELL, S. B
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container_issue 4
container_start_page 1415
container_title Clinical cancer research
container_volume 6
creator SAMIMI, G
FINK, D
VARKI, N. M
HUSAIN, A
HOSKINS, W. J
ALBERTS, D. S
HOWELL, S. B
description Preclinical studies have demonstrated a relationship between DNA mismatch repair (MMR) status and sensitivity to cisplatin and carboplatin. MMR-deficient cells are resistant to both drugs, and selection for cisplatin resistance in vitro is sometimes accompanied by loss of MMR protein expression. We used immunohistochemical staining techniques to investigate hMLH1 and hMSH2 expression in paired ovarian tumor sections from 54 ovarian cancer patients before and after platinum-based therapy. We sought associations between hMLH1 and hMSH2 protein expression and clinical parameters known to be of prognostic significance as well as response to treatment and overall survival. hMLH1 and hMSH2 staining decreased significantly after platinum-based therapy. The percent of malignant cells that stained positive correlated with the intensity of nuclear staining for both proteins; staining for hMLH1 correlated well with staining for hMSH2. Unexpectedly, expression of nuclear hMLH1 correlated negatively with response to treatment. Expression of nuclear hMLH1 and hMSH2 was positively correlated with pretreatment CA125 level, and expression of nuclear hMSH2 was positively correlated with change in CA125 level after treatment. Tumor stage was associated with expression of nuclear hMSH2, and tumor histological subtype was associated with both hMLH1 and hMSH2 staining. No association was found between expression of either protein and overall survival. These results indicate that the tumor is biologically altered after chemotherapy consistent with treatment-induced selection for cells expressing lower hMLH1 and hMSH2 levels. However, immunohistochemical staining for either hMLH1 or hMSH2 was not highly predictive of drug sensitivity as measured by response or survival.
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M ; HUSAIN, A ; HOSKINS, W. J ; ALBERTS, D. S ; HOWELL, S. B</creator><creatorcontrib>SAMIMI, G ; FINK, D ; VARKI, N. M ; HUSAIN, A ; HOSKINS, W. J ; ALBERTS, D. S ; HOWELL, S. B</creatorcontrib><description>Preclinical studies have demonstrated a relationship between DNA mismatch repair (MMR) status and sensitivity to cisplatin and carboplatin. MMR-deficient cells are resistant to both drugs, and selection for cisplatin resistance in vitro is sometimes accompanied by loss of MMR protein expression. We used immunohistochemical staining techniques to investigate hMLH1 and hMSH2 expression in paired ovarian tumor sections from 54 ovarian cancer patients before and after platinum-based therapy. We sought associations between hMLH1 and hMSH2 protein expression and clinical parameters known to be of prognostic significance as well as response to treatment and overall survival. hMLH1 and hMSH2 staining decreased significantly after platinum-based therapy. The percent of malignant cells that stained positive correlated with the intensity of nuclear staining for both proteins; staining for hMLH1 correlated well with staining for hMSH2. Unexpectedly, expression of nuclear hMLH1 correlated negatively with response to treatment. Expression of nuclear hMLH1 and hMSH2 was positively correlated with pretreatment CA125 level, and expression of nuclear hMSH2 was positively correlated with change in CA125 level after treatment. Tumor stage was associated with expression of nuclear hMSH2, and tumor histological subtype was associated with both hMLH1 and hMSH2 staining. No association was found between expression of either protein and overall survival. These results indicate that the tumor is biologically altered after chemotherapy consistent with treatment-induced selection for cells expressing lower hMLH1 and hMSH2 levels. 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Obstetrics ; Humans ; Immunohistochemistry ; Medical sciences ; MutL Protein Homolog 1 ; MutS Homolog 2 Protein ; Neoplasm Proteins - analysis ; Neoplasm Proteins - biosynthesis ; Nuclear Proteins ; Ovarian Neoplasms - drug therapy ; Ovarian Neoplasms - metabolism ; Ovarian Neoplasms - pathology ; Pharmacology. 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Obstetrics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>MutL Protein Homolog 1</subject><subject>MutS Homolog 2 Protein</subject><subject>Neoplasm Proteins - analysis</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Nuclear Proteins</subject><subject>Ovarian Neoplasms - drug therapy</subject><subject>Ovarian Neoplasms - metabolism</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Pharmacology. 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Obstetrics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>MutL Protein Homolog 1</topic><topic>MutS Homolog 2 Protein</topic><topic>Neoplasm Proteins - analysis</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Nuclear Proteins</topic><topic>Ovarian Neoplasms - drug therapy</topic><topic>Ovarian Neoplasms - metabolism</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Pharmacology. Drug treatments</topic><topic>Proto-Oncogene Proteins - analysis</topic><topic>Proto-Oncogene Proteins - biosynthesis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SAMIMI, G</creatorcontrib><creatorcontrib>FINK, D</creatorcontrib><creatorcontrib>VARKI, N. M</creatorcontrib><creatorcontrib>HUSAIN, A</creatorcontrib><creatorcontrib>HOSKINS, W. J</creatorcontrib><creatorcontrib>ALBERTS, D. S</creatorcontrib><creatorcontrib>HOWELL, S. 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ispartof Clinical cancer research, 2000-04, Vol.6 (4), p.1415-1421
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; American Association for Cancer Research; Alma/SFX Local Collection
subjects Adaptor Proteins, Signal Transducing
Antineoplastic agents
Antineoplastic Agents - therapeutic use
Biological and medical sciences
CA-125 Antigen - analysis
Carboplatin - therapeutic use
Carrier Proteins
Chemotherapy
Cisplatin - therapeutic use
Data Interpretation, Statistical
DNA-Binding Proteins
Female
Female genital diseases
Gynecology. Andrology. Obstetrics
Humans
Immunohistochemistry
Medical sciences
MutL Protein Homolog 1
MutS Homolog 2 Protein
Neoplasm Proteins - analysis
Neoplasm Proteins - biosynthesis
Nuclear Proteins
Ovarian Neoplasms - drug therapy
Ovarian Neoplasms - metabolism
Ovarian Neoplasms - pathology
Pharmacology. Drug treatments
Proto-Oncogene Proteins - analysis
Proto-Oncogene Proteins - biosynthesis
Tumors
title Analysis of MLH1 and MSH2 Expression in Ovarian Cancer before and after Platinum Drug-based Chemotherapy
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