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Plasma membrane Ca2+ ATPase isoform 1 down-regulated in human oral cancer

Authors: Kengo, Saito; Katsuhiro, Uzawa; Yosuke, Endo; Yoshikuni, Kato; Dai, Nakashima; Katsunori, Ogawara; Masashi, Shiba; +3 Authors

Plasma membrane Ca2+ ATPase isoform 1 down-regulated in human oral cancer

Abstract

The plasma membrane Ca(2+) ATPase (PMCA) is an essential regulator of free intracellular calcium. Recent studies have reported aberrant expression of the PMCA1 gene, a member of the PMCA family, in several cancer cell types. To elucidate the contribution of PMCA1 to oral carcinogenesis, we analyzed genetic and epigenetic changes and mRNA and protein expression in primary oral squamous cell carcinomas (OSCCs), oral premalignant lesions (OPLs), and OSCC-derived cell lines. The PMCA1 gene was epigenetically inactivated, but not mutated in the eight OSCC-derived cell lines tested. In clinical samples, frequent down-regulation of PMCA1 protein expression was found not only in primary OSCCs (43%), but also in OPLs (40%). Real-time quantitative reverse transcriptase-polymerase chain reaction data were consistent with the protein expression status. These results suggest that inactivation of the PMCA1 gene is a frequent and early event during oral carcinogenesis, and gene expression may be regulated by an epigenetic mechanism.

Related Organizations
Keywords

DNA Mutational Analysis, Down-Regulation, Calcium-Transporting ATPases, DNA Methylation, Immunohistochemistry, Gene Expression Regulation, Neoplastic, Plasma Membrane Calcium-Transporting ATPases, Humans, Mouth Neoplasms, RNA, Messenger, Cation Transport Proteins

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
42
Average
Top 10%
Top 10%
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