The novel ZIP4 regulation and its role in ovarian cancer

Qipeng Fan, Qingchun Cai, Pengfei Li, Wenyan Wang, Jing Wang, Emily Gerry, Tian Li Wang, Ie Ming Shih, Kenneth Nephew, Yan Xu

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Our RNAseq analyses revealed that ZIP4 is a top gene up-regulated in more aggressive ovarian cancer cells. ZIP4's role in cancer stem cells has not been reported in any type of cancer. In addition, the role and regulation of ZIP4, a zinc transporter, have been studied in the context of extracellular zinc transporting. Factors other than zinc with ZIP4 regulatory effects are essentially unknown. ZIP4 expression and its regulation in epithelial ovarian cancer cells was assessed by immunoblotting, quantitative PCR, or immunohistochemistry staining in human ovarian tissues. Cancer stem cell-related activities were examined to evaluate the role of ZIP4 in human highgrade serous ovarian cancer cells in vitro and in vivo. RNAi and CRISPR techniques were used to knockdown or knockout ZIP4 and related genes. Ovarian cancer tissues overexpressed ZIP4 when compared with normal and benign tissues. ZIP4 knockout significantly reduced several cancer stem cell-related activities in EOC cells, including proliferation, anoikis-resistance, colony-formation, spheroid-formation, drug-resistance, and side-population in vitro. ZIP4-expressing side-population highly expressed known CSC markers ALDH1 and OCT4. ZIP4 knockout dramatically reduced tumorigenesis and ZIP4 overexpression increased tumorigenesis in vivo. In addition, the ZIP4-expressing side-population had the tumor initiating activity. Moreover, the oncolipid lysophosphatic acid effectively up-regulated ZIP4 expression via the nuclear receptor peroxisome proliferator-activated receptor gamma and lysophosphatic acid 's promoting effects in cancer stem cell-related activities in HGSOC cells was at least partially mediated by ZIP4 in an extracellular zinc-independent manner. Our critical data imply that ZIP4 is a new and important cancer stem cell regulator in ovarian cancer. Our data also provide an innovative interpretation for the apparent disconnection between low levels of zinc and up-regulation of ZIP4 in ovarian cancer tissues.

Original languageEnglish (US)
Pages (from-to)90090-90107
Number of pages18
JournalOncotarget
Volume8
Issue number52
DOIs
StatePublished - 2017

Fingerprint

Neoplastic Stem Cells
Ovarian Neoplasms
Zinc
Carcinogenesis
Clustered Regularly Interspaced Short Palindromic Repeats
Anoikis
Population
Acids
PPAR gamma
Cytoplasmic and Nuclear Receptors
RNA Interference
Immunoblotting
Drug Resistance
Genes
Neoplasms
Up-Regulation
Immunohistochemistry
Cell Proliferation
Staining and Labeling
Polymerase Chain Reaction

Keywords

  • Cancer stem cells (CSC)
  • LPA
  • Ovarian cancer
  • ZIP4

ASJC Scopus subject areas

  • Oncology

Cite this

Fan, Q., Cai, Q., Li, P., Wang, W., Wang, J., Gerry, E., ... Xu, Y. (2017). The novel ZIP4 regulation and its role in ovarian cancer. Oncotarget, 8(52), 90090-90107. https://doi.org/10.18632/oncotarget.21435

The novel ZIP4 regulation and its role in ovarian cancer. / Fan, Qipeng; Cai, Qingchun; Li, Pengfei; Wang, Wenyan; Wang, Jing; Gerry, Emily; Wang, Tian Li; Shih, Ie Ming; Nephew, Kenneth; Xu, Yan.

In: Oncotarget, Vol. 8, No. 52, 2017, p. 90090-90107.

Research output: Contribution to journalArticle

Fan, Q, Cai, Q, Li, P, Wang, W, Wang, J, Gerry, E, Wang, TL, Shih, IM, Nephew, K & Xu, Y 2017, 'The novel ZIP4 regulation and its role in ovarian cancer', Oncotarget, vol. 8, no. 52, pp. 90090-90107. https://doi.org/10.18632/oncotarget.21435
Fan Q, Cai Q, Li P, Wang W, Wang J, Gerry E et al. The novel ZIP4 regulation and its role in ovarian cancer. Oncotarget. 2017;8(52):90090-90107. https://doi.org/10.18632/oncotarget.21435
Fan, Qipeng ; Cai, Qingchun ; Li, Pengfei ; Wang, Wenyan ; Wang, Jing ; Gerry, Emily ; Wang, Tian Li ; Shih, Ie Ming ; Nephew, Kenneth ; Xu, Yan. / The novel ZIP4 regulation and its role in ovarian cancer. In: Oncotarget. 2017 ; Vol. 8, No. 52. pp. 90090-90107.
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