Expression of 16 kDa proteolipid of vacuolar-type H(+)-ATPase in human pancreatic cancer

Br J Cancer. 1996 Jun;73(12):1511-7. doi: 10.1038/bjc.1996.285.

Abstract

Recent studies have shown that bafilomycin A1-sensitive vacuolar-type H(+)-ATPase (V-ATPase) plays important roles in cell growth and differentiation. However, there is no published study that has focused on the expression of V-ATPase in human tumour tissues. This study was designed to examine the mRNA and protein levels for the 16 kilodalton (kDa) proteolipid of V-ATPase in human pancreatic carcinoma tissues. We first investigated the mRNA level for V-ATPase in six cases of invasive pancreatic cancers and two normal pancreases, using reverse transcription-polymerase chain reaction technique. Then, we examined immunohistochemically the level of V-ATPase protein in 49 pancreatic cancers and ten benign cystic neoplasms of the pancreas, using antisera raised against the 16 kDa proteolipid. There was a notable difference in the level of V-ATPase mRNA between normal and pancreatic carcinoma tissues, with no evident difference in the expression of the beta-actin gene. Immunohistochemically, 42 out of 46 invasive ductal cancers (92%) displayed a mild to marked immunoreactivity for V-ATPase in the cytoplasm, whereas neither non-invasive ductal cancers nor benign cystic neoplasms expressed detectable immunoreactive proteins. These findings suggest that the overexpression of V-ATPase protein is characteristic of invasive pancreatic tumours. V-ATPase may play some crucial roles in tumour progression.

MeSH terms

  • Adenocarcinoma / enzymology*
  • Adenocarcinoma / pathology
  • Adult
  • Aged
  • Amino Acid Sequence
  • Base Sequence
  • Carcinoma, Ductal, Breast / enzymology*
  • Carcinoma, Ductal, Breast / pathology
  • Disease Progression
  • Female
  • Humans
  • Macromolecular Substances
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Pancreas / enzymology
  • Pancreatic Neoplasms / enzymology*
  • Pancreatic Neoplasms / pathology
  • Proteolipids / biosynthesis*
  • Proton-Translocating ATPases / biosynthesis*
  • Proton-Translocating ATPases / immunology
  • RNA, Messenger / metabolism*
  • Reference Values
  • Vacuoles / enzymology

Substances

  • Macromolecular Substances
  • Proteolipids
  • RNA, Messenger
  • Proton-Translocating ATPases