2. Academic Validation
  3. SIK2 maintains breast cancer stemness by phosphorylating LRP6 and activating Wnt/β-catenin signaling

SIK2 maintains breast cancer stemness by phosphorylating LRP6 and activating Wnt/β-catenin signaling

  • Oncogene. 2022 Apr;41(16):2390-2403. doi: 10.1038/s41388-022-02259-0.
Zhuoxian Rong 1 2 3 4 5,  Lu Zhang 1 2,  Zhi Li 1 2 3 4 5,  Zhi Xiao 6,  Yumei Duan 7,  Xinxin Ren 1 2,  Yuyuan Zi 1 2,  Jie Gao 1 2,  Yun Mu 1 2,  Yidi Guan 1 2,  Zhen Cao 1 2,  Xitao Wang 1 2,  Qian Pei 1 2,  Yu Zeng 1 2,  Qi Fan 1 2,  Zimei Zeng 1 2,  Danmin Ou 1 2,  Jiang He 1 2 3,  Yingjie Nie 8,  Rong Tan 1 2 3 4 5,  Liang Weng 1 2 3 4 5,  Yuhao Li 9,  Rong Xiang 9,  Yuezhen Deng 10 11 12 13 14,  Lunquan Sun 15 16 17 18 19
Affiliations

Affiliations

  • 1 Xiangya Cancer Center, Xiangya Hospital, Central South University, Changsha, 410008, China.
  • 2 Key Laboratory of Molecular Radiation Oncology Hunan Province, Changsha, 410008, China.
  • 3 Institute of Gerontological Cancer Research, National Clinical Research Center for Gerontology, Changsha, 410008, China.
  • 4 Hunan International Science and Technology Collaboration Base of Precision Medicine for Cancer, Changsha, 410008, China.
  • 5 Center for Molecular Imaging of Central South University, Xiangya Hospital, Changsha, 410008, China.
  • 6 Deparment of Breast Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
  • 7 Department of Pathology, Xiangya Hospital, Central South University, Changsha, 410008, China.
  • 8 NHC Key Laboratory of Pulmonary Immune-related Diseases, Guizhou Provincial People's Hospital, Guiyang, 550000, China.
  • 9 College of Medicine, Nankai University, 94 Weijin Road, Tianjin, 300071, China.
  • 10 Xiangya Cancer Center, Xiangya Hospital, Central South University, Changsha, 410008, China. [email protected].
  • 11 Key Laboratory of Molecular Radiation Oncology Hunan Province, Changsha, 410008, China. [email protected].
  • 12 Institute of Gerontological Cancer Research, National Clinical Research Center for Gerontology, Changsha, 410008, China. [email protected].
  • 13 Hunan International Science and Technology Collaboration Base of Precision Medicine for Cancer, Changsha, 410008, China. [email protected].
  • 14 Center for Molecular Imaging of Central South University, Xiangya Hospital, Changsha, 410008, China. [email protected].
  • 15 Xiangya Cancer Center, Xiangya Hospital, Central South University, Changsha, 410008, China. [email protected].
  • 16 Key Laboratory of Molecular Radiation Oncology Hunan Province, Changsha, 410008, China. [email protected].
  • 17 Institute of Gerontological Cancer Research, National Clinical Research Center for Gerontology, Changsha, 410008, China. [email protected].
  • 18 Hunan International Science and Technology Collaboration Base of Precision Medicine for Cancer, Changsha, 410008, China. [email protected].
  • 19 Center for Molecular Imaging of Central South University, Xiangya Hospital, Changsha, 410008, China. [email protected].
PMID: 35277657 DOI: 10.1038/s41388-022-02259-0
Abstract

Breast Cancer Stem Cells (BCSCs) are the main drivers of recurrence and metastasis. However, commonly used drugs rarely target BCSCs. Via screenings, we found that Salt-inducible kinase 2 (SIK2) participated in breast Cancer (BC) stemness maintenance and zebrafish embryos development. SIK2 was upregulated in recurrence samples. Knockdown of SIK2 expression reduced the proportion of BCSCs and the tumor initiation of BC cells. Mechanistically, SIK2, phosphorylated by CK1α, directly phosphorylated LRP6 in a SIK2 kinase activity-dependent manner, leading to Wnt/β-catenin signaling pathway activation. ARN-3236 and HG-9-91-01, inhibitors of SIK2, inhibited LRP6 phosphorylation and β-catenin accumulation and disturbed stemness maintenance. In addition, the SIK2-activated Wnt/β-catenin signaling led to induction of IDH1 expression, causing metabolic reprogramming in BC cells. These findings demonstrate a novel mechanism whereby Wnt/β-catenin signaling pathway is regulated by different kinases in response to metabolic requirement of CSCs, and suggest that SIK2 inhibition may potentially be a strategy for eliminating BCSCs.

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