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ATPase family AAA domain-containing 3A is a novel anti-apoptotic factor in lung adenocarcinoma cells.

Abstract
AAA domain-containing 3A (ATAD3A) is a member of the AAA-ATPase family. Three forms of ATAD3 have been identified: ATAD3A, ATAD3B and ATAD3C. In this study, we examined the type and expression of ATAD3 in lung adenocarcinoma (LADC). Expression of ATAD3A was detected by reverse transcription-polymerase chain reaction, immunoblotting, immunohistochemistry and confocal immunofluorescent microscopy. Our results show that ATAD3A is the major form expressed in LADC. Silencing of ATAD3A expression increased mitochondrial fragmentation and cisplatin sensitivity. Serum deprivation increased ATAD3A expression and drug resistance. These results suggest that ATAD3A could be an anti-apoptotic marker in LADC.
AuthorsHsin-Yuan Fang, Chia-Ling Chang, Shu-Han Hsu, Chih-Yang Huang, Shu-Fen Chiang, Shiow-Her Chiou, Chun-Hua Huang, Yi-Ting Hsiao, Tze-Yi Lin, I-Ping Chiang, Wen-Hu Hsu, Sumio Sugano, Chih-Yi Chen, Ching-Yuang Lin, Wen-Je Ko, Kuan-Chih Chow
JournalJournal of cell science (J Cell Sci) Vol. 123 Issue Pt 7 Pg. 1171-80 (Apr 01 2010) ISSN: 1477-9137 [Electronic] England
PMID20332122 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • ATAD3A protein, human
  • Apoptosis Regulatory Proteins
  • Membrane Proteins
  • Mitochondrial Proteins
  • RNA, Small Interfering
  • Adenosine Triphosphatases
  • ATPases Associated with Diverse Cellular Activities
  • Cisplatin
Topics
  • ATPases Associated with Diverse Cellular Activities
  • Adenocarcinoma (drug therapy, genetics, metabolism, pathology)
  • Adenosine Triphosphatases (genetics, metabolism)
  • Apoptosis (drug effects, genetics)
  • Apoptosis Regulatory Proteins (genetics, metabolism)
  • Cisplatin (pharmacology)
  • Disease Progression
  • Drug Resistance (genetics)
  • Female
  • HeLa Cells
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms (drug therapy, genetics, metabolism, pathology)
  • Male
  • Membrane Proteins (genetics, metabolism)
  • Microscopy, Fluorescence
  • Mitochondria (drug effects, genetics, ultrastructure)
  • Mitochondrial Proteins (genetics, metabolism)
  • Neoplasm Staging
  • RNA, Small Interfering (genetics)
  • Sequence Analysis, DNA

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