Mesothelin is Commonly Expressed in Pancreatic Adenocarcinoma but Unrelated to Cancer Aggressiveness

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Mesothelin is Commonly Expressed in Pancreatic Adenocarcinoma but Unrelated to Cancer Aggressiveness. / Weidemann, Sören; Perez, Daniel; Izbicki, Jakob R; Neipp, Michael; Mofid, Hamid; Daniels, Thies; Nahrstedt, Ulf; Jacobsen, Frank; Bernreuther, Christian; Simon, Ronald; Steurer, Stefan; Burandt, Eike; Marx, Andreas H; Krech, Till; Clauditz, Till S; Jansen, Kristina.

In: CANCER INVEST, Vol. 39, No. 9, 10.2021, p. 711-720.

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@article{d716b58580ed4d4784ca97572eb6b6bc,
title = "Mesothelin is Commonly Expressed in Pancreatic Adenocarcinoma but Unrelated to Cancer Aggressiveness",
abstract = "Data on Mesothelin (MSLN) expression in human normal and cancerous tissues is controversial. We employed immunohistochemistry (IHC) on a tissue microarray (TMA) from 599 pancreatic cancers and 12 large tissue sections of pancreatitis. MSLN expression was highest in pancreatic adenocarcinomas (89%) and adenocarcinomas of the ampulla Vateri (79%), infrequent in pancreatitis and absent in 6 acinus cell carcinomas and normal pancreas. MSLN expression was unrelated to pathological tumor stage, grade, metastasis, and tumor-infiltrating CD8+ lymphocytes. In conclusion, pancreatic cancer may be ideally suited for putative anti- MSLN therapies, and MSLN may represent a suitable biomarker for pancreatic cancer diagnosis, especially on small biopsies.",
author = "S{\"o}ren Weidemann and Daniel Perez and Izbicki, {Jakob R} and Michael Neipp and Hamid Mofid and Thies Daniels and Ulf Nahrstedt and Frank Jacobsen and Christian Bernreuther and Ronald Simon and Stefan Steurer and Eike Burandt and Marx, {Andreas H} and Till Krech and Clauditz, {Till S} and Kristina Jansen",
year = "2021",
month = oct,
doi = "10.1080/07357907.2021.1943747",
language = "English",
volume = "39",
pages = "711--720",
journal = "CANCER INVEST",
issn = "0735-7907",
publisher = "informa healthcare",
number = "9",

}

RIS

TY - JOUR

T1 - Mesothelin is Commonly Expressed in Pancreatic Adenocarcinoma but Unrelated to Cancer Aggressiveness

AU - Weidemann, Sören

AU - Perez, Daniel

AU - Izbicki, Jakob R

AU - Neipp, Michael

AU - Mofid, Hamid

AU - Daniels, Thies

AU - Nahrstedt, Ulf

AU - Jacobsen, Frank

AU - Bernreuther, Christian

AU - Simon, Ronald

AU - Steurer, Stefan

AU - Burandt, Eike

AU - Marx, Andreas H

AU - Krech, Till

AU - Clauditz, Till S

AU - Jansen, Kristina

PY - 2021/10

Y1 - 2021/10

N2 - Data on Mesothelin (MSLN) expression in human normal and cancerous tissues is controversial. We employed immunohistochemistry (IHC) on a tissue microarray (TMA) from 599 pancreatic cancers and 12 large tissue sections of pancreatitis. MSLN expression was highest in pancreatic adenocarcinomas (89%) and adenocarcinomas of the ampulla Vateri (79%), infrequent in pancreatitis and absent in 6 acinus cell carcinomas and normal pancreas. MSLN expression was unrelated to pathological tumor stage, grade, metastasis, and tumor-infiltrating CD8+ lymphocytes. In conclusion, pancreatic cancer may be ideally suited for putative anti- MSLN therapies, and MSLN may represent a suitable biomarker for pancreatic cancer diagnosis, especially on small biopsies.

AB - Data on Mesothelin (MSLN) expression in human normal and cancerous tissues is controversial. We employed immunohistochemistry (IHC) on a tissue microarray (TMA) from 599 pancreatic cancers and 12 large tissue sections of pancreatitis. MSLN expression was highest in pancreatic adenocarcinomas (89%) and adenocarcinomas of the ampulla Vateri (79%), infrequent in pancreatitis and absent in 6 acinus cell carcinomas and normal pancreas. MSLN expression was unrelated to pathological tumor stage, grade, metastasis, and tumor-infiltrating CD8+ lymphocytes. In conclusion, pancreatic cancer may be ideally suited for putative anti- MSLN therapies, and MSLN may represent a suitable biomarker for pancreatic cancer diagnosis, especially on small biopsies.

U2 - 10.1080/07357907.2021.1943747

DO - 10.1080/07357907.2021.1943747

M3 - SCORING: Journal article

C2 - 34143695

VL - 39

SP - 711

EP - 720

JO - CANCER INVEST

JF - CANCER INVEST

SN - 0735-7907

IS - 9

ER -