TY - JOUR
T1 - Adenosquamous Carcinoma of the Pancreas
T2 - Molecular Characterization of 23 Patients Along With A Literature Review
AU - Borazanci, Erkut
AU - Millis, Sherri Z.
AU - Korn, Ron
AU - Han, Haiyong
AU - Whatcott, Clifford J.
AU - Gatalica, Zoran
AU - Barrett, Michael T.
AU - Cridebring, Derek
AU - Von Hoff, Daniel D.
N1 - Funding Information:
Supported by In part the Lee T. Hanley Fund for Pancreatic Cancer Research.
Publisher Copyright:
© 2020. The Author(s) 2015. Published by Baishideng Publishing Group Inc. All Rights Reserved.
PY - 2015/9/15
Y1 - 2015/9/15
N2 - Adenosquamous carcinoma of the pancreas (ASCP) is a rare entity. Like adenocarcinoma of the pancreas, overall survival is poor. Characteristics of ASCP include central tumor necrosis, along with osteoclasts and hypercalcemia. Various theories exist as to why this histological subtype exists, as normal pancreas tissue has no benign squamous epithelium. Due to the rarity of this disease, limited molecular analysis has been performed, and those reports indicate unique molecular features of ASCP. In this paper, we characterize 23 patients diagnosed with ASCP through molecular profiling using immunohistochemistry staining, fluorescent in situ hybridization, chromogenic in situ hybridization, and gene sequencing, Additionally, we provide a comprehensive literature review of what is known to date of ASCP. Molecular characterization revealed overexpression in MRP1 (80%), MGMT (79%), TOP2A (75), RRM1 (42%), TOPO1 (42%), PTEN (45%), CMET (40%), and C-KIT (10%) among others. One hundred percent of samples tested were positive for KRAS mutations. This analysis shows heretofore unsuspected leads to be considered for treatments of this rare type of exocrine pancreas cancer. Molecular profiling may be appropriate to provide maximum information regarding the patient's tumor. Further work should be pursued to better characterize this disease.
AB - Adenosquamous carcinoma of the pancreas (ASCP) is a rare entity. Like adenocarcinoma of the pancreas, overall survival is poor. Characteristics of ASCP include central tumor necrosis, along with osteoclasts and hypercalcemia. Various theories exist as to why this histological subtype exists, as normal pancreas tissue has no benign squamous epithelium. Due to the rarity of this disease, limited molecular analysis has been performed, and those reports indicate unique molecular features of ASCP. In this paper, we characterize 23 patients diagnosed with ASCP through molecular profiling using immunohistochemistry staining, fluorescent in situ hybridization, chromogenic in situ hybridization, and gene sequencing, Additionally, we provide a comprehensive literature review of what is known to date of ASCP. Molecular characterization revealed overexpression in MRP1 (80%), MGMT (79%), TOP2A (75), RRM1 (42%), TOPO1 (42%), PTEN (45%), CMET (40%), and C-KIT (10%) among others. One hundred percent of samples tested were positive for KRAS mutations. This analysis shows heretofore unsuspected leads to be considered for treatments of this rare type of exocrine pancreas cancer. Molecular profiling may be appropriate to provide maximum information regarding the patient's tumor. Further work should be pursued to better characterize this disease.
KW - Adenosquamous carcinoma of the pancreas
KW - Molecular profiling
KW - Review
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U2 - 10.4251/wjgo.v7.i9.132
DO - 10.4251/wjgo.v7.i9.132
M3 - Article
AN - SCOPUS:84992701765
SN - 1948-5204
VL - 7
SP - 132
EP - 140
JO - World Journal of Gastrointestinal Oncology
JF - World Journal of Gastrointestinal Oncology
IS - 9
ER -