Glycoconjugated Metallohelices Eliminate Cancer Stem‐Like Cells via Modulating G‐Quadruplex Surrounding Transcriptional Start Site of Sox2 Gene

H Hongshuang Qin (Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin 130022 P.R. China) J Jie Yang T Tingting Cui (Key Laboratory for Medicinal Resources and Natural Pharmaceutical Chemistry, Ministry of Education, College of Life Sciences, Shaanxi Normal University) H Hualong Song (Department of Chemistry) M Miles Postings (Department of Chemistry) P Peter Scott (Department of Chemistry) C Chunyu Wang (Center for Biotechnology and Interdisciplinary Studies) C Chuanqi Zhao (Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization) J Jinsong Ren (Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization) X Xiaogang Qu (Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization)

Abstract

Abstract As an important pluripotency transcription factor, Sox2 plays key roles in the stemness maintenance of cancer stem‐like cells (CSCs). Here, we found that a highly conserved G‐rich region surrounding transcriptional start sites (TSSs) of Sox2 gene can form G‐quadruplex (Sox2G4) both in vitro and in cells. More intriguingly, the glycoconjugated triplex metallohelice [Fe 2 L Δ‐f 3 ] 4+ (Δ‐f) can enantioselectively stabilize Sox2G4. Sox2G4 stabilization induced by [Fe 2 L Δ‐f 3 ] 4+ (Δ‐f) rather than Λ‐f results in inhibition of Sox2 expression both in mRNA and protein levels in breast CSCs and decreases the cell viability and stemness of breast CSCs. These results indicate that [Fe 2 L Δ‐f 3 ] 4+ (Δ‐f) has the enantioselectivity even in living cells. In vivo studies further demonstrate that Δ‐f can reduce tumor initiation of breast CSCs. To our knowledge, this is the first report that targeting G‐quadruplexes of pluripotency genes can regulate the fates of CSCs. Our work provides a new way to target CSC gene and eradicate cancer stem cells.

Article Details

Volume / Issue Vol. 64, Issue 37
Published September 08, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

H

Hongshuang Qin

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun Jilin 130022 P.R. China

J

Jie Yang

T

Tingting Cui

Key Laboratory for Medicinal Resources and Natural Pharmaceutical Chemistry, Ministry of Education, College of Life Sciences, Shaanxi Normal University

H

Hualong Song

Department of Chemistry

M

Miles Postings

Department of Chemistry

P

Peter Scott

Department of Chemistry

C

Chunyu Wang

Center for Biotechnology and Interdisciplinary Studies

C

Chuanqi Zhao

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization

J

Jinsong Ren

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization

X

Xiaogang Qu

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization