4.3 Article

Down-regulation of LAPTM5 in human cancer cells

Journal

ONCOTARGET
Volume 7, Issue 19, Pages 28320-28328

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.8614

Keywords

LAPTM5; ESCC; tumor suppressor genes; lysosomes; cell death

Funding

  1. Japan Society for the Promotion of Science (JSPS) [25250019, 24590372, 22134002]
  2. Project for Development of Innovative Research on Cancer Therapeutics (P-Direct)
  3. Tailor-Made Medical Treatment
  4. BioBank Japan Project (BBJ) from The Japan Agency for Medical Research and Development
  5. Global Center of Excellence (GCOE) Program from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan
  6. Foundation for Promotion of Cancer Research from the Ministry of Health, Labour and Welfare (MHLW), Japan
  7. Grants-in-Aid for Scientific Research [15H05908, 25250019, 24590372] Funding Source: KAKEN

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Lysosomal-associated protein multispanning transmembrane 5 (LAPTM5) is a membrane protein that localizes to intracellular vesicles. It has been previously demonstrated that LAPTM5 expression level is decreased in neuroblastoma (NB) cells, and excessive accumulation of LAPTM5 was shown to induce lysosomal cell death in these cells. However, the pathological expression and role of LAPTM5 in other types of human cancers are largely unknown. Here, we found that LAPTM5 mRNA level is frequently decreased in various cancer cell lines, and its low expression in patients with esophageal squamous cell carcinoma (ESCC) and non-small cell lung cancer (NSCLC) was significantly correlated with poor prognosis. Furthermore, we showed that overexpression of LAPTM5 in several cancer cells induces lysosomal cell death due to lysosomal destabilization, indicated by leakage of lysosomal cathepsin D into the cytosol as well as impairment of autophagy. These findings suggest that the inactivation of LAPTM5 may contribute to tumorigenesis in a subset of human cancers.

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