“…In addition to normal and diseased tissues, numerous recent studies have revealed UCN I is expressed in various cancer cells and cell lines, including human glioblastoma cells (KSN42, T98G, RT2, 9L, A172, and U-138 MG cells) [62] , pituitary adenoma cells [44,63] , malignant melanoma cells [42] , both thyroid carcinoma and pheochromocytoma (multiple endocrine neoplasia type II) cells [64] , breast cancer cells [65] , gastric adenocarcinoma cells and the STKM-1 cell line [66,67] , primary and metastatic liver carcinoma cells [22] , pancreatic ductal adenocarcinoma cells and neoplasms [68] , the MIN6 insulinoma cell line [33] , clear cell renal cell carcinoma cells [51] , NCI-H295R human adrenal carcinoma cells [69] , human endometrial carcinoma cells [70] , and human prostate adenocarcinoma cells [59] . Interestingly, UCN I and its working receptors (CRFR1 and CRFR2) do not always co-localize; for example, they do not colocalize in RT2 and 9L human glioblastoma cells [62] .…”