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Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer.


ABSTRACT: Tetrathiomolybdate (TM) is a novel, copper-depleting compound associated with promising survival in a phase II study of patients with high-risk and triple-negative breast cancer. We sought to elucidate the mechanism of TM by exploring its effects on collagen processing and immune function in the tumor microenvironment (TME). Using an exploratory cohort, we identified markers of collagen processing (LOXL2, PRO-C3, C6M, and C1M) that differed between those with breast cancer versus controls. We measured these collagen biomarkers in TM-treated patients on the phase II study and detected evidence of decreased collagen cross-linking and increased degradation over formation in those without disease compared to those who experienced disease progression. Preclinical studies revealed decreased collagen deposition, lower levels of myeloid-derived suppressor cells, and higher CD4+ T-cell infiltration in TM-treated mice compared with controls. This study reveals novel mechanisms of TM targeting the TME and immune response with potential applications across cancer types.

SUBMITTER: Liu YL 

PROVIDER: S-EPMC8382701 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer.

Liu Ying L YL   Bager Cecilie Liv CL   Willumsen Nicholas N   Ramchandani Divya D   Kornhauser Naomi N   Ling Lu L   Cobham Marta M   Andreopoulou Eleni E   Cigler Tessa T   Moore Anne A   LaPolla Dayle D   Fitzpatrick Veronica V   Ward Maureen M   Warren J David JD   Fischbach Claudia C   Mittal Vivek V   Vahdat Linda T LT  

NPJ breast cancer 20210823 1


Tetrathiomolybdate (TM) is a novel, copper-depleting compound associated with promising survival in a phase II study of patients with high-risk and triple-negative breast cancer. We sought to elucidate the mechanism of TM by exploring its effects on collagen processing and immune function in the tumor microenvironment (TME). Using an exploratory cohort, we identified markers of collagen processing (LOXL2, PRO-C3, C6M, and C1M) that differed between those with breast cancer versus controls. We me  ...[more]

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