PCDH10 is required for the tumorigenicity of glioblastoma cells
Creators
- Echizen, Kanae1
- Nakada, Mitsutoshi2
- Hayashi, Tomoatsu1
- Sabit, Hemragul2
- Furuta, Takuya2
- Nakai, Miyuki1
- Koyama-Nasu, Ryo1
- Nishimura, Yukiko1
- Taniue, Kenzui1
- Morishita, Yasuyuki3
- Hirano, Shinji4
- Terai, Kenta5
- Todo, Tomoki6
- Ino, Yasushi6
- Mukasa, Akitake6
- Takayanagi, Shunsaku6
- Ohtani, Ryohei6
- Saito, Nobuhito6
- Akiyama, Tetsu1
- 1. Laboratory of Molecular and Genetic Information, Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1, Yayoi, Bunkyo-ku, Tokyo 113-0032 (Japan)
- 2. Department of Neurosurgery, Graduate School of Medical Science, Kanazawa University, 13-1, Takara-machi, Kanazawa 920-8641 (Japan)
- 3. Department of Molecular Pathology, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan)
- 4. Department of Neurobiology and Anatomy, Kochi Medical School, Kochi University, Okoh-cho, Nangoku-City, Kochi 783-8505 (Japan)
- 5. Laboratory of Function and Morphology, Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1, Yayoi, Bunkyo-ku, Tokyo 113-0032 (Japan)
- 6. Department of Neurosurgery, Faculty of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8655 (Japan)
Description
Highlights: • PCDH10 is required for the proliferation, survival and self-renewal of glioblastoma cells. • PCDH10 is required for glioblastoma cell migration and invasion. • PCDH10 is required for the tumorigenicity of glioblastoma cells. • PCDH10 may be a promising target for the therapy of glioblastoma. - Abstract: Protocadherin10 (PCDH10)/OL-protocadherin is a cadherin-related transmembrane protein that has multiple roles in the brain, including facilitating specific cell–cell connections, cell migration and axon guidance. It has recently been reported that PCDH10 functions as a tumor suppressor and that its overexpression inhibits proliferation or invasion of multiple tumor cells. However, the function of PCDH10 in glioblastoma cells has not been elucidated. In contrast to previous reports on other tumors, we show here that suppression of the expression of PCDH10 by RNA interference (RNAi) induces the growth arrest and apoptosis of glioblastoma cells in vitro. Furthermore, we demonstrate that knockdown of PCDH10 inhibits the growth of glioblastoma cells xenografted into immunocompromised mice. These results suggest that PCDH10 is required for the proliferation and tumorigenicity of glioblastoma cells. We speculate that PCDH10 may be a promising target for the therapy of glioblastoma
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2013.12.138Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2013.12.138;
- PII
- S0006-291X(13)02209-2;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 444
- Journal Issue
- 1
- Journal Page Range
- p. 13-18
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46122141
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- APOPTOSIS; BRAIN; GLIOMAS; IN VITRO; INHIBITION; INTERFERENCE; JOINTS; MICE; NERVE CELLS; PROLIFERATION; RNA; THERAPY; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; ANIMALS; BODY; CENTRAL NERVOUS SYSTEM; DISEASES; MAMMALS; MEDICINE; NEOPLASMS; NERVOUS SYSTEM; NERVOUS SYSTEM DISEASES; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANS; RODENTS; SOMATIC CELLS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.