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ID3 is a novel target gene of p53 and modulates lung cancer cell metastasis.
Nagasaka, Mai; Miyajima, Chiharu; Inoue, Yasumichi; Hashiguchi, Sakura; Suzuki, Yuya; Morishita, Daisuke; Aoki, Hiromasa; Toriuchi, Kohki; Katayama, Ryohei; Aoyama, Mineyoshi; Hayashi, Hidetoshi.
Affiliation
  • Nagasaka M; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Miyajima C; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Inoue Y; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan. Electronic address: yainoue@phar.nagoya-cu.ac.jp.
  • Hashiguchi S; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Suzuki Y; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Morishita D; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Aoki H; Department of Pathobiology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Toriuchi K; Department of Pathobiology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Katayama R; Division of Experimental Chemotherapy, Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, 135-8550, Japan.
  • Aoyama M; Department of Pathobiology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.
  • Hayashi H; Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan. Electronic address: hhayashi@phar.nagoya-cu.ac.jp.
Biochem Biophys Res Commun ; 708: 149789, 2024 05 14.
Article in En | MEDLINE | ID: mdl-38513475
ABSTRACT
The tumor suppressor p53 prevents cancer development by regulating dozens of target genes with diverse biological functions. Although numerous p53 target genes have been identified to date, the dynamics and function of the regulatory network centered on p53 have not yet been fully elucidated. We herein identified inhibitor of DNA-binding/differentiation-3 (ID3) as a direct p53 target gene. p53 bound the distal promoter of ID3 and positively regulated its transcription. ID3 expression was significantly decreased in clinical lung cancer tissues, and was closely associated with overall survival outcomes in these patients. Functionally, ID3 deficiency promoted the metastatic ability of lung cancer cells through its effects on the transcriptional regulation of CDH1. Furthermore, the ectopic expression of ID3 in p53-knockdown cells restored E-cadherin expression. Collectively, the present results demonstrate that ID3 plays a tumor-suppressive role as a downstream effector of p53 and impedes lung cancer cell metastasis by regulating E-cadherin expression.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lung Neoplasms Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2024 Document type: Article Affiliation country: Japón Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lung Neoplasms Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2024 Document type: Article Affiliation country: Japón Country of publication: Estados Unidos