Extrachromosomal DNA of the symbiont Sodalis glossinidius
JOURNAL OF BACTERIOLOGY
Authors: Darby, AC; Lagnel, J; Matthew, CZ; Bourtzis, K; Maudlin, I; Welburn, SC
Abstract
The extrachromosomal DNA of Sodalis glossinidius from two tsetse fly species was sequenced and contained four circular elements: three plasmids, pSG1 (82 kb), pSG2 (27 kb), and pSG4 (11 kb), and a bacteriophage-like pSG3 (19 kb) element. The information suggests S. glossinidius is evolving towards an obligate association with tsetse flies.
Pregnancy Specific beta-1 Glycoprotein 1 is Expressed in Pancreatic Ductal Adenocarcinoma and its Subcellular Localization Correlates with Overall Survival
JOURNAL OF CANCER
Authors: Shahinian, Jasmin H.; Fuellgraf, Hannah; Tholen, Stefan; Mastroianni, Justin; Knopf, Julia Daniela; Kuehs, Markus; Mayer, Bettina; Schlimpert, Manuel; Kulemann, Birte; Kuesters, Simon; Hoeppner, Jens; Wellner, Ulrich F.; Werner, Martin; Hopt, Ulrich T.; Zeiser, Robert; Bronsert, Peter; Schilling, Oliver
Abstract
Proteins of the pregnancy specific beta-1 glycoprotein (PSG) family are renowned for their elevated expression during pregnancy. Only few reports have investigated their expression in adenocarcinomas. We studied the expression of PSG1 in pancreatic adenocarcinoma (PDAC). In a cohort of 104 patient samples, immunohistochemical analysis determined PSG1 expression in every specimen. PSG1 was found at apical and cytoplasmic localization or solely at cytoplasmic localization, with the latter case being correlated to shortened median survival (25 vs 11 months, logrank p-value < 0.001). At the same time, enzyme linked immunosorbent assay (ELISA) did not detect elevated PSG1 levels in the plasma of PDAC patients as opposed to the plasma of healthy, non-pregnant control individuals. We also probed the impact of PSG1 expression in a murine tumor model system, using subcutaneous injection of Colo-26 cells into immunocompetent BALB/c mice. Here, tumor growth was not affected by the expression of human PSG1. Our study reaffirms interest into the tumor-contextual biology of PSG proteins.