Dnajb8, a Member of the Heat Shock Protein 40 Family Has a Role in the Tumor Initiation and Resistance to Docetaxel but Is Dispensable for Stress Response

PLoS One. 2016 Jan 11;11(1):e0146501. doi: 10.1371/journal.pone.0146501. eCollection 2016.

Abstract

Cancer stem-like cells (CSCs)/cancer-initiating cells (CICs) are defined by their abilities of tumor initiation, self-renewal and differentiation. In a previous study, we showed by gene knockdown using siRNA and gene overexpression experiments that Dnaj (Hsp40) homolog, subfamily B, member 8 (DNAJB8), a role in the maintenance, of renal cell carcinoma CSCs/CICs. In the present study, we established Dnajb8 knockout (KO) renal cell carcinoma (RCC) line cells (RenCa cells) and analyzed the cells to confirm the function of Dnajb8 in RCC CSCs/CICs. Dnajb8 KO cells showed reduced ratios of side population cells and reduced sphere forming ability. An in vivo single cell tumor initiation assay revealed that the numbers of CSCs/CICs were 3 in 4 wild-type RenCa cells and 1 in 4 Dnajb8 KO cells. Dnajb8 KO cells showed sensitivity to Docetaxel. On the other hand, Dnajb8 KO cells did not show any sensitivities to stresses including low pH, low glucose, heat shock and sensitivity to cisplatin. The results indicate that Dnajb8 has a role in tumor initiation, side population ratio and sphere formation but it is dispensable for stress responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Base Sequence
  • CRISPR-Cas Systems
  • Carcinoma, Renal Cell / pathology
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic / metabolism
  • Cisplatin / therapeutic use
  • Docetaxel
  • Drug Resistance, Neoplasm
  • Female
  • Gene Knockout Techniques
  • Glucose / chemistry
  • HSP40 Heat-Shock Proteins / metabolism*
  • Humans
  • Hydrogen-Ion Concentration
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / metabolism*
  • Kidney Neoplasms / pathology
  • Mice
  • Mice, Inbred BALB C
  • Molecular Chaperones / metabolism
  • Molecular Sequence Data
  • Neoplasm Transplantation
  • Neoplastic Stem Cells / cytology
  • Nerve Tissue Proteins / metabolism
  • RNA, Small Interfering / metabolism
  • Side-Population Cells / metabolism
  • Stress, Physiological
  • Taxoids / therapeutic use*

Substances

  • Antineoplastic Agents
  • DNAJB8 protein, human
  • Dnajb8 protein, mouse
  • HSP40 Heat-Shock Proteins
  • Molecular Chaperones
  • Nerve Tissue Proteins
  • RNA, Small Interfering
  • Taxoids
  • Docetaxel
  • Glucose
  • Cisplatin

Grants and funding

This study was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to NS), program for developing the supporting system for upgrading education and research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to NS) and Takeda Science Foundation (to YH), Sagawa Foundation for Promotion of Cancer Research (to YH), Suharakinenzaidan Co., Ltd. (to Y.H.) and Kobayashi foundation for cancer research (to YH). This study was supported in part by Grants-in-Aid for Regional R&D Proposal-Based Program from Northern Advancement Center for Science & Technology of Hokkaido Japan (to YH and TT). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.