Radiation-Induced RhoGDIβ Cleavage Leads to Perturbation of Cell Polarity: A Possible Link to Cancer Spreading

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Mamoru Fujiwara - , Prefectural University of Hiroshima (Autor:in)
  • Mayumi Okamoto - , Prefectural University of Hiroshima (Autor:in)
  • Masato Hori - , Prefectural University of Hiroshima (Autor:in)
  • Hiroshi Suga - , Prefectural University of Hiroshima (Autor:in)
  • Hiroshi Jikihara - , Prefectural University of Hiroshima (Autor:in)
  • Yuka Sugihara - , Prefectural University of Hiroshima (Autor:in)
  • Fumio Shimamoto - , Prefectural University of Hiroshima (Autor:in)
  • Toshio Mori - , Nara Medical University (Autor:in)
  • Koichi Nakaoji - , Abbott Laboratories (Autor:in)
  • Kazuhiko Hamada - , Abbott Laboratories (Autor:in)
  • Takahide Ota - , Kanazawa Medical University (Autor:in)
  • Ralf Wiedemuth - , Klinik und Poliklinik für Neurochirurgie, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Achim Temme - , Klinik und Poliklinik für Neurochirurgie (Autor:in)
  • Masaaki Tatsuka - , Prefectural University of Hiroshima (Autor:in)

Abstract

The equilibrium between proliferation and apoptosis is tightly balanced to maintain tissue homeostasis in normal tissues and even in tumors. Achieving and maintaining such a balance is important for cancer regrowth and spreading after cytotoxic treatments. Caspase-3 activation and tumor cell death following anticancer therapy as well as accompanying cell death pathways are well characterized, but their association to homeostasis of cancerous tissue and tumor progression remains poorly understood. Here we proposed a novel mechanism of cancer spreading induced by caspase-3. RhoGDIβ, known as a direct cleavage substrate of caspase-3, is overexpressed in many epithelial cancers. The N-terminal-truncated RhoGDIβ (ΔN-RhoGDIβ) is accumulated in caspase-3-activated cells. Stable expression of ΔN-RhoGDIβ in HeLa cells did not induce apoptosis, but impaired directional cell migration in a wound-healing assay accompanied by a perturbed direction of cell division at the wound edge. Subcellular protein fractionation experiments revealed that ΔN-RhoGDIβ but not wild-type RhoGDIβ was present in the detergent-soluble cytoplasmic and nuclear fractions and preferentially associated with Cdc42. Furthermore, Cdc42 activity was constitutively inhibited by stable expression of ΔN-RhoGDIβ, resulting in increased radiation-induced compensatory proliferation linking to RhoA activation. Thus, ΔN-RhoGDIβ dominant-negatively regulates Cdc42 activity and contributes to loss of polarity-related functions. The caspase-3-cleaved RhoGDIβ is a possible determinant to promote cancer spreading due to deregulation of directional organization of tumor cell population and inhibition of default equilibrium between proliferation and apoptosis after cytotoxic damage. J. Cell. Physiol. 231: 2493-2505, 2016. © 2016 Wiley Periodicals, Inc.

Details

OriginalspracheEnglisch
Seiten (von - bis)2493-505
Seitenumfang13
FachzeitschriftJournal of cellular physiology
Jahrgang231
Ausgabenummer11
PublikationsstatusVeröffentlicht - Nov. 2016
Peer-Review-StatusJa

Externe IDs

Scopus 84978372411

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Apoptosis/radiation effects, Caspase 3/metabolism, Cell Division/radiation effects, Cell Movement/radiation effects, Cell Polarity/radiation effects, Cell Proliferation/radiation effects, Cell Survival/radiation effects, Down-Regulation/radiation effects, Enzyme Activation/radiation effects, Genes, Dominant, HeLa Cells, Humans, Models, Biological, Mutant Proteins/metabolism, Neoplasm Metastasis, Neoplasms/pathology, Protein Transport/radiation effects, Radiation, Subcellular Fractions/metabolism, X-Rays, cdc42 GTP-Binding Protein/metabolism, rho Guanine Nucleotide Dissociation Inhibitor beta/metabolism