Assessment of cholecystokinin 2 receptor (CCK2R) in neoplastic tissue

Jyoti Roy1,2, Karson S Putt1, Domenico Coppola3

  • 1Center for Drug Discovery, Purdue University, West Lafayette, IN 47907 USA.

Oncotarget
|February 25, 2016
PubMed

Insights

Cholecystokinin 2 receptor (CCK2R) is found in most cancers and normal tissues. This study found no significant difference in CCK2R expression between tested cancer types and normal tissues.

Area of Science:

  • Oncology
  • Molecular Biology
  • Gastroenterology

Background:

  • Cholecystokinin 2 receptor (CCK2R) expression is reported in various cancers, including colorectal, liver, lung, pancreatic, ovarian, stomach, thyroid, and neuroendocrine tumors.
  • Some studies indicate CCK2R overexpression in specific cancers (colorectal, lung, pancreas, thyroid) compared to normal tissues, driving development of targeted agents.
  • A comprehensive comparative analysis of CCK2R expression across multiple cancer types and normal tissues was lacking.

Purpose of the Study:

  • To conduct a comprehensive immunohistochemical analysis comparing CCK2R expression in multiple cancer types versus multiple normal tissues.
  • To determine if specific cancer types exhibit statistically significant overexpression of CCK2R compared to all normal tissues.

Main Methods:

  • Immunohistochemical analysis was performed on cancer samples: gastrointestinal stromal tumor (GIST), hepatocellular carcinoma (HCC), non-small cell lung cancer (NSCLC), pancreatic adenocarcinoma, and thyroid cancer.
  • Normal tissue samples from esophagus, liver, lung, pancreas, stomach, spleen, and thyroid were analyzed for CCK2R expression.
  • Statistical comparison of CCK2R expression levels between cancer and normal tissue groups was conducted.

Main Results:

  • CCK2R expression was detected in nearly all tested cancer samples and normal tissue samples.
  • No statistically significant difference was found where cancer samples showed greater CCK2R expression than all normal samples.
  • The study did not identify a universal overexpression of CCK2R in the tested cancers compared to all normal tissues.

Conclusions:

  • CCK2R is broadly expressed in both cancerous and normal tissues within the studied sample set.
  • The findings do not support the hypothesis of statistically significant CCK2R overexpression in these specific cancers over all normal tissues.
  • This comprehensive analysis suggests that CCK2R expression patterns may not be a universally distinguishing feature for targeted therapies across all tested cancer types.

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