The E3 ligase APC/CCdh1 promotes ubiquitylation-mediated proteolysis of PAX3 to suppress melanocyte proliferation and melanoma growth

Juxiang Cao, Xiangpeng Dai, Lixin Wan, Hongshen Wang, Jinfang Zhang, Philip S. Goff, Elena V. Sviderskaya, Zhenyu Xuan, Zhixiang Xu, Xiaowei Xu, Philip Hinds, Keith T. Flaherty, Douglas V. Faller, Colin R. Goding, Yongjun Wang, Wenyi Wei, Rutao Cui

Research output: Contribution to journalArticle

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Abstract

The anaphase-promoting complex or cyclosome with the subunit Cdh1 (APC/CCdh1) is an E3 ubiquitin ligase involved in the control of the cell cycle.Here, weidentified sporadicmutations occurring in the genes encoding APC components, including Cdh1, in human melanoma samples and found that loss of APC/ CCdh1 may promote melanoma development and progression, but not by affecting cell cycle regulatory targets of APC/C. Most of the mutations we found in CDH1 were those associated with ultraviolet light (UV)-inducedmelanomagenesis.Compared with normal human skin tissue and human ormousemelanocytes, the abundance of Cdh1 was decreased and that of the transcription factor PAX3 was increased in human melanoma tissue and human or mouse melanoma cell lines, respectively; Cdh1 abundance was further decreased with advanced stages ofhumanmelanoma. PAX3was a substrate of APC/CCdh1 in melanocytes, and APC/CCdh1-mediated ubiquitylation marked PAX3 for proteolytic degradation in a manner dependent on theD-boxmotif inPAX3. Eithermutating theD-box inPAX3 or knocking downCdh1 prevented the ubiquitylation and degradation of PAX3 and increased proliferation and melanin production in melanocytes. Knocking down Cdh1 in melanoma cells in culture or before implantation in mice promoted doxorubicin resistance, whereas reexpressing wild-type Cdh1, but not E3 ligase-deficient Cdh1 or a mutant that could not interact with PAX3, restored doxorubicin sensitivity in melanoma cells both in culture and in xenografts. Thus, our findings suggest a tumor suppressor role for APC/CCdh1 in melanocytes and that targeting PAX3 may be a strategy for treating melanoma.

Original languageEnglish (US)
Article numberra87
JournalScience Signaling
Volume8
Issue number392
DOIs
StatePublished - Sep 1 2015
Externally publishedYes

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Proteolysis
Ubiquitin-Protein Ligases
Ubiquitination
Melanocytes
Melanoma
Cells
Doxorubicin
Growth
Anaphase-Promoting Complex-Cyclosome
Tissue
Degradation
Gene encoding
Melanins
Heterografts
Tumors
Skin
Transcription Factors
APC Genes
Substrates
Ultraviolet Rays

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

The E3 ligase APC/CCdh1 promotes ubiquitylation-mediated proteolysis of PAX3 to suppress melanocyte proliferation and melanoma growth. / Cao, Juxiang; Dai, Xiangpeng; Wan, Lixin; Wang, Hongshen; Zhang, Jinfang; Goff, Philip S.; Sviderskaya, Elena V.; Xuan, Zhenyu; Xu, Zhixiang; Xu, Xiaowei; Hinds, Philip; Flaherty, Keith T.; Faller, Douglas V.; Goding, Colin R.; Wang, Yongjun; Wei, Wenyi; Cui, Rutao.

In: Science Signaling, Vol. 8, No. 392, ra87, 01.09.2015.

Research output: Contribution to journalArticle

Cao, J, Dai, X, Wan, L, Wang, H, Zhang, J, Goff, PS, Sviderskaya, EV, Xuan, Z, Xu, Z, Xu, X, Hinds, P, Flaherty, KT, Faller, DV, Goding, CR, Wang, Y, Wei, W & Cui, R 2015, 'The E3 ligase APC/CCdh1 promotes ubiquitylation-mediated proteolysis of PAX3 to suppress melanocyte proliferation and melanoma growth', Science Signaling, vol. 8, no. 392, ra87. https://doi.org/10.1126/scisignal.aab1995
Cao, Juxiang ; Dai, Xiangpeng ; Wan, Lixin ; Wang, Hongshen ; Zhang, Jinfang ; Goff, Philip S. ; Sviderskaya, Elena V. ; Xuan, Zhenyu ; Xu, Zhixiang ; Xu, Xiaowei ; Hinds, Philip ; Flaherty, Keith T. ; Faller, Douglas V. ; Goding, Colin R. ; Wang, Yongjun ; Wei, Wenyi ; Cui, Rutao. / The E3 ligase APC/CCdh1 promotes ubiquitylation-mediated proteolysis of PAX3 to suppress melanocyte proliferation and melanoma growth. In: Science Signaling. 2015 ; Vol. 8, No. 392.
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abstract = "The anaphase-promoting complex or cyclosome with the subunit Cdh1 (APC/CCdh1) is an E3 ubiquitin ligase involved in the control of the cell cycle.Here, weidentified sporadicmutations occurring in the genes encoding APC components, including Cdh1, in human melanoma samples and found that loss of APC/ CCdh1 may promote melanoma development and progression, but not by affecting cell cycle regulatory targets of APC/C. Most of the mutations we found in CDH1 were those associated with ultraviolet light (UV)-inducedmelanomagenesis.Compared with normal human skin tissue and human ormousemelanocytes, the abundance of Cdh1 was decreased and that of the transcription factor PAX3 was increased in human melanoma tissue and human or mouse melanoma cell lines, respectively; Cdh1 abundance was further decreased with advanced stages ofhumanmelanoma. PAX3was a substrate of APC/CCdh1 in melanocytes, and APC/CCdh1-mediated ubiquitylation marked PAX3 for proteolytic degradation in a manner dependent on theD-boxmotif inPAX3. Eithermutating theD-box inPAX3 or knocking downCdh1 prevented the ubiquitylation and degradation of PAX3 and increased proliferation and melanin production in melanocytes. Knocking down Cdh1 in melanoma cells in culture or before implantation in mice promoted doxorubicin resistance, whereas reexpressing wild-type Cdh1, but not E3 ligase-deficient Cdh1 or a mutant that could not interact with PAX3, restored doxorubicin sensitivity in melanoma cells both in culture and in xenografts. Thus, our findings suggest a tumor suppressor role for APC/CCdh1 in melanocytes and that targeting PAX3 may be a strategy for treating melanoma.",
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