Cited by 134Cancer-related Molecular PathwaysCell death mechanisms and regulationMechanisms of cancer metastasis

Programmed Cell Death Protein 4 Down-regulates Y-Box Binding Protein-1 Expression via a Direct Interaction with Twist1 to Suppress Cancer Cell Growth

Shiota, Masaki, Izumi, Hiroto, Tanimoto, Akihide, Takahashi, Mayu, Miyamoto, Naoya, Kashiwagi, Eiji, Kidani, Akihiko, Hirano, Gen +7 more·2009·Cancer Research

Abstract

Programmed cell death protein 4 (PDCD4) has recently been shown to be involved in both transcription and translation, and to regulate cell growth. However, the mechanisms underlying PDCD4 function are not well understood. In this study, we show that PDCD4 interacts directly with the transcription factor Twist1 and leads to reduced cell growth through the down-regulation of the Twist1 target gene Y-box binding protein-1 (YB-1). PDCD4 interacts with the DNA binding domain of Twist1, inhibiting its DNA binding ability and YB-1 expression. Immunohistochemical analysis showed that an inverse correlation between nuclear PDCD4 and YB-1 expression levels was observed in 37 clinical prostate cancer specimens. Growth suppression by PDCD4 expression was completely recovered by either Twist1 or YB-1 expression. Moreover, PDCD4-overexpressing cells are sensitive to cisplatin and paclitaxel but not to etoposide or 5-fluorouracil. In summary, PDCD4 negatively regulates YB-1 expression via its interaction with Twist1 and is involved in cancer cell growth and chemoresistance. [Cancer Res 2009;69(7):3148–56]

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Crossref · 10.1158/0008-5472.can-08-2334

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  • PDCD4 interacts directly with the transcription factor TWIST1 and leads to inhibition of cell growth via down-regulation of the TWIST1 target gene YB-1.

    “For examples, PDCD4 interacts directly with the transcription factor TWIST 1 and leads to the inhibition of cell growth via the down-regulation of the TWIST 1 target gene Y-box binding protein-1 (YB-1) [38].”
  • In the case of Twist1, unlike p65, the functionally significant binding to PDCD4 occurs in the nucleus.

    “In the case of Twist1, unlike p65, the functionally significant binding to PDCD4 occurs in the nucleus.”
  • PDCD4 directly interacts with the helix-loop-helix DNA-binding domain of Twist1 to inhibit its binding to the promoter of Y-box-binding protein (YB-1) to consequently downregulate YB-1 mRNA expression in prostate cancer cells.

    “PDCD4 directly interacts with the helix-loop-helix DNA-binding domain of Twist1 to inhibit its binding to the promoter of Y-box-binding protein (YB-1) to consequently downregulate YB-1 mRNA expression in prostate cancer cells (38).”

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References 36 · Cited by 134

Authors
Shiota, M., Izumi, H., Tanimoto, A., Takahashi, M., Miyamoto, N., Kashiwagi, E., Kidani, A., Hirano, G., Masubuchi, D., Fukunaka, Y., Yasuniwa, Y., Naito, S., Nishizawa, S., Sasaguri, Y., & Kohno, K.
Affiliations
  • Kyushu University (JP)
  • 1Molecular Biology, Departments of
  • 2Pathology II, and
  • University of Occupational and Environmental Health Japan (JP)
Venue
Cancer Research
Published
2009-04-01
Volume
69
Issue
7
Pages
3148-3156
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2149193228
Cited by
134
References
36
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 3 · 2021: 7 · 2020: 7 · 2019: 7 · 2018: 9 · 2017: 4 · 2016: 5 · 2015: 8 · 2014: 17 · 2013: 14 · 2012: 9
FWCI
7.28
Type
journal article
Language
en
Open access
closed
Locations
  • Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
Keywords
PDCD4, YB-1, TWIST1, protein-protein interaction, transcriptional repression, tumor cell growth inhibition, prostate cancer, chemoresistance, cisplatin sensitivity, paclitaxel sensitivity, DNA binding inhibition
MeSH terms
Cisplatin, Glioma, Humans, Male, Nuclear Proteins, Prostatic Neoplasms, Transcription, Genetic, Transfection, Down-Regulation, RNA-Binding Proteins, Paclitaxel, Cell Line, Tumor, Cell Growth Processes, Apoptosis Regulatory Proteins, Y-Box-Binding Protein 1, Twist-Related Protein 1

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