2. Academic Validation
  3. Targeting tumor hypoxia inhibits aggressive phenotype of dedifferentiated thyroid cancer

Targeting tumor hypoxia inhibits aggressive phenotype of dedifferentiated thyroid cancer

  • J Clin Endocrinol Metab. 2022 Oct 3;dgac548. doi: 10.1210/clinem/dgac548.
Ben Ma 1 2,  Shishuai Wen 3,  Yi Luo 1 2,  Tingting Zhang 1 2,  Yichen Yang 1 2,  Cenkai Shen 1 2,  Yan Zhang 2 4,  Qinghai Ji 1 2,  Ning Qu 1 2,  Yu Wang 1 2
Affiliations

Affiliations

  • 1 Department of Head and Neck Surgery, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
  • 2 Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, People's Republic of China.
  • 3 Department of thyroid surgery, Zhejiang University, School of Medicine, the first affiliated hospital, Hangzhou, People's Republic of China.
  • 4 Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China.
PMID: 36190930 DOI: 10.1210/clinem/dgac548
Abstract

Background: Hypoxia is commonly observed in multiple aggressive cancers. It remains unclear concerning hypoxia's roles in tumor biology and therapy of dedifferentiated thyroid Cancer (DDTC).

Materials and methods: We discovered and confirmed hypoxia's correlation with dedifferentiation status, poor prognoses and immune checkpoints in thyroid Cancer using transcriptome data from our center and Gene Expression Omnibus (GEO) database. Then, the effect of targeting hypoxia was investigated via treating anaplastic thyroid Cancer (ATC) cells with acriflavine (ACF) in vitro and in vivo, and hypoxia was analyzed for its association with response to immunotherapy in patients.

Results: Hypoxia score was positively associated with dedifferentiation status, and high hypoxia score significantly correlated with reduced overall survival, TP53 mutation and elevated expression of immunosuppression-related markers in DDTC. ACF and siRNA targeting HIF-1α significantly suppressed growth and proliferation of thyroid Cancer cells in vitro and in vivo, and reduced c-Myc and PDL1 expression in ATC. HIF-1α showed a positive correlation with PDL1 expression in DDTC. Integrated analyses of phospho-proteome and RNA-sequencing data revealed that ACF's target was connected with differentiation genes and immune checkpoints via tumor-related kinases in ATC. Furthermore, hypoxia score was associated with immunotherapeutic response in some Cancer types.

Conclusions: Hypoxia score serves as a significant indicator for dedifferentiation status, prognoses and immunotherapeutic response predicted by Tumor Immune Dysfunction and Exclusion in DDTC patients. Targeting hypoxia by ACF is useful to alleviate aggressive phenotype of ATC in pre-clinical model of DDTC.

Keywords

DDTC; TME; acriflavine; hypoxia; immunotherapy.

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