Squalene synthase induces tumor necrosis factor receptor 1 enrichment in lipid rafts to promote lung cancer metastasis

Yi Fang Yang, Yi Hua Jan, Yu Peng Liu, Chih Jen Yang, Chia Yi Su, Yu Chan Chang, Tsung Ching Lai, Jean Chiou, Hong Yuan Tsai, Jean Lu, Chia Ning Shen, Jin Yuh Shew, Pei Jung Lu, Yuan Feng Lin, Ming Shyan Huang, Michael Hsiao

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Rationale: Metabolic alterations contribute to cancer development and progression. However, the molecular mechanisms relating metabolism to cancer metastasis remain largely unknown. Objectives: To identify a key metabolic enzyme that is aberrantly overexpressed in invasive lung cancer cells and to investigate its functional role and prognostic value in lung cancer. Methods: The differential expression of metabolic enzymes in noninvasive CL1-0 cells and invasive CL1-5 cells was analyzed by a gene expression microarray. The expression of target genes in clinical specimens from patients with lung cancer was examined by immunohistochemistry. Pharmacologic and gene knockdown/overexpression approaches were used to investigate the function of the target gene during invasion and metastasis in vitro and in vivo. The association between the target gene expression and clinicopathologic parameters was further analyzed. Bioinformatic analyses were used to discover the signaling pathways involved in target gene-regulated invasion and migration. Measurements and Main Results: Squalene synthase (SQS) was up-regulated in CL1-5 cells and in the tumor regions of the lung cancer specimens. Loss of function or knockdown of SQS significantly inhibited invasion/migration and metastasis in cell and animal models and vice versa. High expression of SQS was significantly associated with poor prognosis among patients with lung cancer. Mechanistically, SQS contributed to a lipid-raft-localized enrichment of tumor necrosis factor receptor 1 in a cholesterol-dependentmanner, which resulted in the enhancement of nuclear factor-κB activation leading to matrix metallopeptidase 1 up-regulation. Conclusions: Up-regulation of SQS promotes metastasis of lung cancer by enhancing tumor necrosis factor-α receptor 1 and nuclear factor-κB activation and matrix metallopeptidase 1 expression. Targeting SQS may have considerable potential as a novel therapeutic strategy to treat metastatic lung cancer.

Original languageEnglish
Pages (from-to)675-687
Number of pages13
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume190
Issue number6
DOIs
Publication statusPublished - Sep 15 2014

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Farnesyl-Diphosphate Farnesyltransferase
Tumor Necrosis Factor Receptors
Lung Neoplasms
Neoplasm Metastasis
Lipids
Gene Expression
Up-Regulation
Gene Knockdown Techniques
Neoplasms
Enzymes
Computational Biology
Genes
Animal Models
Immunohistochemistry
Cholesterol

Keywords

  • Cholesterol
  • Lung cancer metastasis
  • Squalene synthase
  • TNFR1

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine
  • Medicine(all)

Cite this

Squalene synthase induces tumor necrosis factor receptor 1 enrichment in lipid rafts to promote lung cancer metastasis. / Yang, Yi Fang; Jan, Yi Hua; Liu, Yu Peng; Yang, Chih Jen; Su, Chia Yi; Chang, Yu Chan; Lai, Tsung Ching; Chiou, Jean; Tsai, Hong Yuan; Lu, Jean; Shen, Chia Ning; Shew, Jin Yuh; Lu, Pei Jung; Lin, Yuan Feng; Huang, Ming Shyan; Hsiao, Michael.

In: American Journal of Respiratory and Critical Care Medicine, Vol. 190, No. 6, 15.09.2014, p. 675-687.

Research output: Contribution to journalArticle

Yang, YF, Jan, YH, Liu, YP, Yang, CJ, Su, CY, Chang, YC, Lai, TC, Chiou, J, Tsai, HY, Lu, J, Shen, CN, Shew, JY, Lu, PJ, Lin, YF, Huang, MS & Hsiao, M 2014, 'Squalene synthase induces tumor necrosis factor receptor 1 enrichment in lipid rafts to promote lung cancer metastasis', American Journal of Respiratory and Critical Care Medicine, vol. 190, no. 6, pp. 675-687. https://doi.org/10.1164/rccm.201404-0714OC
Yang, Yi Fang ; Jan, Yi Hua ; Liu, Yu Peng ; Yang, Chih Jen ; Su, Chia Yi ; Chang, Yu Chan ; Lai, Tsung Ching ; Chiou, Jean ; Tsai, Hong Yuan ; Lu, Jean ; Shen, Chia Ning ; Shew, Jin Yuh ; Lu, Pei Jung ; Lin, Yuan Feng ; Huang, Ming Shyan ; Hsiao, Michael. / Squalene synthase induces tumor necrosis factor receptor 1 enrichment in lipid rafts to promote lung cancer metastasis. In: American Journal of Respiratory and Critical Care Medicine. 2014 ; Vol. 190, No. 6. pp. 675-687.
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abstract = "Rationale: Metabolic alterations contribute to cancer development and progression. However, the molecular mechanisms relating metabolism to cancer metastasis remain largely unknown. Objectives: To identify a key metabolic enzyme that is aberrantly overexpressed in invasive lung cancer cells and to investigate its functional role and prognostic value in lung cancer. Methods: The differential expression of metabolic enzymes in noninvasive CL1-0 cells and invasive CL1-5 cells was analyzed by a gene expression microarray. The expression of target genes in clinical specimens from patients with lung cancer was examined by immunohistochemistry. Pharmacologic and gene knockdown/overexpression approaches were used to investigate the function of the target gene during invasion and metastasis in vitro and in vivo. The association between the target gene expression and clinicopathologic parameters was further analyzed. Bioinformatic analyses were used to discover the signaling pathways involved in target gene-regulated invasion and migration. Measurements and Main Results: Squalene synthase (SQS) was up-regulated in CL1-5 cells and in the tumor regions of the lung cancer specimens. Loss of function or knockdown of SQS significantly inhibited invasion/migration and metastasis in cell and animal models and vice versa. High expression of SQS was significantly associated with poor prognosis among patients with lung cancer. Mechanistically, SQS contributed to a lipid-raft-localized enrichment of tumor necrosis factor receptor 1 in a cholesterol-dependentmanner, which resulted in the enhancement of nuclear factor-κB activation leading to matrix metallopeptidase 1 up-regulation. Conclusions: Up-regulation of SQS promotes metastasis of lung cancer by enhancing tumor necrosis factor-α receptor 1 and nuclear factor-κB activation and matrix metallopeptidase 1 expression. Targeting SQS may have considerable potential as a novel therapeutic strategy to treat metastatic lung cancer.",
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AU - Su, Chia Yi

AU - Chang, Yu Chan

AU - Lai, Tsung Ching

AU - Chiou, Jean

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N2 - Rationale: Metabolic alterations contribute to cancer development and progression. However, the molecular mechanisms relating metabolism to cancer metastasis remain largely unknown. Objectives: To identify a key metabolic enzyme that is aberrantly overexpressed in invasive lung cancer cells and to investigate its functional role and prognostic value in lung cancer. Methods: The differential expression of metabolic enzymes in noninvasive CL1-0 cells and invasive CL1-5 cells was analyzed by a gene expression microarray. The expression of target genes in clinical specimens from patients with lung cancer was examined by immunohistochemistry. Pharmacologic and gene knockdown/overexpression approaches were used to investigate the function of the target gene during invasion and metastasis in vitro and in vivo. The association between the target gene expression and clinicopathologic parameters was further analyzed. Bioinformatic analyses were used to discover the signaling pathways involved in target gene-regulated invasion and migration. Measurements and Main Results: Squalene synthase (SQS) was up-regulated in CL1-5 cells and in the tumor regions of the lung cancer specimens. Loss of function or knockdown of SQS significantly inhibited invasion/migration and metastasis in cell and animal models and vice versa. High expression of SQS was significantly associated with poor prognosis among patients with lung cancer. Mechanistically, SQS contributed to a lipid-raft-localized enrichment of tumor necrosis factor receptor 1 in a cholesterol-dependentmanner, which resulted in the enhancement of nuclear factor-κB activation leading to matrix metallopeptidase 1 up-regulation. Conclusions: Up-regulation of SQS promotes metastasis of lung cancer by enhancing tumor necrosis factor-α receptor 1 and nuclear factor-κB activation and matrix metallopeptidase 1 expression. Targeting SQS may have considerable potential as a novel therapeutic strategy to treat metastatic lung cancer.

AB - Rationale: Metabolic alterations contribute to cancer development and progression. However, the molecular mechanisms relating metabolism to cancer metastasis remain largely unknown. Objectives: To identify a key metabolic enzyme that is aberrantly overexpressed in invasive lung cancer cells and to investigate its functional role and prognostic value in lung cancer. Methods: The differential expression of metabolic enzymes in noninvasive CL1-0 cells and invasive CL1-5 cells was analyzed by a gene expression microarray. The expression of target genes in clinical specimens from patients with lung cancer was examined by immunohistochemistry. Pharmacologic and gene knockdown/overexpression approaches were used to investigate the function of the target gene during invasion and metastasis in vitro and in vivo. The association between the target gene expression and clinicopathologic parameters was further analyzed. Bioinformatic analyses were used to discover the signaling pathways involved in target gene-regulated invasion and migration. Measurements and Main Results: Squalene synthase (SQS) was up-regulated in CL1-5 cells and in the tumor regions of the lung cancer specimens. Loss of function or knockdown of SQS significantly inhibited invasion/migration and metastasis in cell and animal models and vice versa. High expression of SQS was significantly associated with poor prognosis among patients with lung cancer. Mechanistically, SQS contributed to a lipid-raft-localized enrichment of tumor necrosis factor receptor 1 in a cholesterol-dependentmanner, which resulted in the enhancement of nuclear factor-κB activation leading to matrix metallopeptidase 1 up-regulation. Conclusions: Up-regulation of SQS promotes metastasis of lung cancer by enhancing tumor necrosis factor-α receptor 1 and nuclear factor-κB activation and matrix metallopeptidase 1 expression. Targeting SQS may have considerable potential as a novel therapeutic strategy to treat metastatic lung cancer.

KW - Cholesterol

KW - Lung cancer metastasis

KW - Squalene synthase

KW - TNFR1

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