MUC5AC expression is linked to mucinous/endometroid subtype, absence of nodal metastasis and mismatch repair deficiency in ovarian cancer

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MUC5AC expression is linked to mucinous/endometroid subtype, absence of nodal metastasis and mismatch repair deficiency in ovarian cancer. / Rico, Sebastian Dwertmann; Schmalfeldt, Barbara; Müller, Volkmar; Wölber, Linn; Witzel, Isabell; Paluchowski, Peter; von Leffern, Ingo; Heilenkötter, Uwe; Jacobsen, Frank; Bernreuther, Christian; Clauditz, Till; Simon, Ronald; Steurer, Stefan; Burandt, Eike; Marx, Andreas H; Krech, Till.

in: PATHOL RES PRACT, Jahrgang 224, 153533, 08.2021.

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@article{b6a66ec4bc174012aa585583cd362755,
title = "MUC5AC expression is linked to mucinous/endometroid subtype, absence of nodal metastasis and mismatch repair deficiency in ovarian cancer",
abstract = "Mucin 5AC (MUC5AC) is a secreted gel-forming mucin which is expressed by mucus producing cells of several organs but can also be found in cancer cells of the ovary, pancreas, and gastrointestinal tract. This study aimed to characterize the expression of MUC5AC and its potential prognostic implications in different ovarian cancer subtypes. MUC5AC expression was analyzed by immunohistochemistry on a tissue microarray containing 603 ovarian cancers. MUC5AC was commonly expressed in mucinous (27/36; 75%) and endometrioid (12/39; 31%) carcinomas, whereas malignant mixed Mullerian tumors (2/27; 7%), high-grade serous (20/373; 5%) and clear cell carcinomas (1/28; 4%) were only rarely MUC5AC positive and also showed lower expression levels. MUC5AC positive endometroid carcinomas and high-grade serous carcinomas lacked lymph node metastases (p = 0.0495 and p = 0.0216) suggesting a more favorable prognosis. Deficient mismatch repair (dMMR), associated with a favorable prognosis in different cancer types, was found in 4/39 (10%) MUC5AC positive cancers but in only 5/375 (1%) of MUC5AC negative cancers (p = 0.0052). In subgroup analyses MUC5AC positive endometroid carcinomas more frequently showed dMMR (4/10; 40%) as opposed to MUC5AC negative endometroid carcinomas (3/23; 13%; p = 0.0932). In summary, the results of our study show that MUC5AC expression is associated with mucinous and endometrioid ovarian carcinomas, lack of nodal metastases and dMMR. MUC5AC expressing ovarian cancers should be evaluated for dMMR.",
author = "Rico, {Sebastian Dwertmann} and Barbara Schmalfeldt and Volkmar M{\"u}ller and Linn W{\"o}lber and Isabell Witzel and Peter Paluchowski and {von Leffern}, Ingo and Uwe Heilenk{\"o}tter and Frank Jacobsen and Christian Bernreuther and Till Clauditz and Ronald Simon and Stefan Steurer and Eike Burandt and Marx, {Andreas H} and Till Krech",
note = "Copyright {\textcopyright} 2021. Published by Elsevier GmbH.",
year = "2021",
month = aug,
doi = "10.1016/j.prp.2021.153533",
language = "English",
volume = "224",
journal = "PATHOL RES PRACT",
issn = "0344-0338",
publisher = "Urban und Fischer Verlag GmbH und Co. KG",

}

RIS

TY - JOUR

T1 - MUC5AC expression is linked to mucinous/endometroid subtype, absence of nodal metastasis and mismatch repair deficiency in ovarian cancer

AU - Rico, Sebastian Dwertmann

AU - Schmalfeldt, Barbara

AU - Müller, Volkmar

AU - Wölber, Linn

AU - Witzel, Isabell

AU - Paluchowski, Peter

AU - von Leffern, Ingo

AU - Heilenkötter, Uwe

AU - Jacobsen, Frank

AU - Bernreuther, Christian

AU - Clauditz, Till

AU - Simon, Ronald

AU - Steurer, Stefan

AU - Burandt, Eike

AU - Marx, Andreas H

AU - Krech, Till

N1 - Copyright © 2021. Published by Elsevier GmbH.

PY - 2021/8

Y1 - 2021/8

N2 - Mucin 5AC (MUC5AC) is a secreted gel-forming mucin which is expressed by mucus producing cells of several organs but can also be found in cancer cells of the ovary, pancreas, and gastrointestinal tract. This study aimed to characterize the expression of MUC5AC and its potential prognostic implications in different ovarian cancer subtypes. MUC5AC expression was analyzed by immunohistochemistry on a tissue microarray containing 603 ovarian cancers. MUC5AC was commonly expressed in mucinous (27/36; 75%) and endometrioid (12/39; 31%) carcinomas, whereas malignant mixed Mullerian tumors (2/27; 7%), high-grade serous (20/373; 5%) and clear cell carcinomas (1/28; 4%) were only rarely MUC5AC positive and also showed lower expression levels. MUC5AC positive endometroid carcinomas and high-grade serous carcinomas lacked lymph node metastases (p = 0.0495 and p = 0.0216) suggesting a more favorable prognosis. Deficient mismatch repair (dMMR), associated with a favorable prognosis in different cancer types, was found in 4/39 (10%) MUC5AC positive cancers but in only 5/375 (1%) of MUC5AC negative cancers (p = 0.0052). In subgroup analyses MUC5AC positive endometroid carcinomas more frequently showed dMMR (4/10; 40%) as opposed to MUC5AC negative endometroid carcinomas (3/23; 13%; p = 0.0932). In summary, the results of our study show that MUC5AC expression is associated with mucinous and endometrioid ovarian carcinomas, lack of nodal metastases and dMMR. MUC5AC expressing ovarian cancers should be evaluated for dMMR.

AB - Mucin 5AC (MUC5AC) is a secreted gel-forming mucin which is expressed by mucus producing cells of several organs but can also be found in cancer cells of the ovary, pancreas, and gastrointestinal tract. This study aimed to characterize the expression of MUC5AC and its potential prognostic implications in different ovarian cancer subtypes. MUC5AC expression was analyzed by immunohistochemistry on a tissue microarray containing 603 ovarian cancers. MUC5AC was commonly expressed in mucinous (27/36; 75%) and endometrioid (12/39; 31%) carcinomas, whereas malignant mixed Mullerian tumors (2/27; 7%), high-grade serous (20/373; 5%) and clear cell carcinomas (1/28; 4%) were only rarely MUC5AC positive and also showed lower expression levels. MUC5AC positive endometroid carcinomas and high-grade serous carcinomas lacked lymph node metastases (p = 0.0495 and p = 0.0216) suggesting a more favorable prognosis. Deficient mismatch repair (dMMR), associated with a favorable prognosis in different cancer types, was found in 4/39 (10%) MUC5AC positive cancers but in only 5/375 (1%) of MUC5AC negative cancers (p = 0.0052). In subgroup analyses MUC5AC positive endometroid carcinomas more frequently showed dMMR (4/10; 40%) as opposed to MUC5AC negative endometroid carcinomas (3/23; 13%; p = 0.0932). In summary, the results of our study show that MUC5AC expression is associated with mucinous and endometrioid ovarian carcinomas, lack of nodal metastases and dMMR. MUC5AC expressing ovarian cancers should be evaluated for dMMR.

U2 - 10.1016/j.prp.2021.153533

DO - 10.1016/j.prp.2021.153533

M3 - SCORING: Journal article

C2 - 34171599

VL - 224

JO - PATHOL RES PRACT

JF - PATHOL RES PRACT

SN - 0344-0338

M1 - 153533

ER -