Premium
Soluble MICA is elevated in pancreatic cancer: Results from a population based case‐control study
Author(s) -
Onyeaghala Guillaume,
Nelson Heather H.,
Thyagarajan Bharat,
Linabery Amy M.,
PanoskaltsisMortari Angela,
Gross Myron,
Anderson Kristin E.,
Prizment Anna E.
Publication year - 2017
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.22667
Subject(s) - pancreatic cancer , odds ratio , biology , logistic regression , medicine , cancer , confidence interval , population , case control study , oncology , gastroenterology , environmental health
Pancreatic cancer is diagnosed at a late stage and has one of the highest cancer mortality rates in the United States, creating an urgent need for novel early detection tools. A candidate biomarker for use in early detection is the soluble MHC class I‐related chain A (s‐MICA) ligand, which pancreatic tumors shed to escape immune detection. The objective of this study was to define the association between s‐MICA levels and pancreatic cancer, in a population‐based case‐control study. S‐MICA was measured in 143 pancreatic cancer cases and 459 controls. Unconditional logistic regression was used to calculate odds ratio (OR) for pancreatic cancer and 95% confidence intervals (CI). There was a positive association between increasing s‐MICA levels and pancreatic cancer: compared to the lowest tertile, the ORs for pancreatic cancer were 1.25 (95%CI: 0.75‐2.07) and 2.10 (95%CI: 1.29‐3.42) in the second and highest tertiles, respectively ( P ‐trend = 0.02). Our study supports previous work demonstrating a positive association between plasma s‐MICA levels and pancreatic cancer.