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 i...

Full description

Bibliographic Details
Main Authors: Ying L. Liu, Cecilie Liv Bager, Nicholas Willumsen, Divya Ramchandani, Naomi Kornhauser, Lu Ling, Marta Cobham, Eleni Andreopoulou, Tessa Cigler, Anne Moore, Dayle LaPolla, Veronica Fitzpatrick, Maureen Ward, J. David Warren, Claudia Fischbach, Vivek Mittal, Linda T. Vahdat
Format: Article
Language:English
Published: Nature Publishing Group 2021-08-01
Series:npj Breast Cancer
Online Access:https://doi.org/10.1038/s41523-021-00313-w
id doaj-37a653a1d4054f088c420dae713f918a
record_format Article
spelling doaj-37a653a1d4054f088c420dae713f918a2021-08-29T11:34:24ZengNature Publishing Groupnpj Breast Cancer2374-46772021-08-017111110.1038/s41523-021-00313-wTetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancerYing L. Liu0Cecilie Liv Bager1Nicholas Willumsen2Divya Ramchandani3Naomi Kornhauser4Lu Ling5Marta Cobham6Eleni Andreopoulou7Tessa Cigler8Anne Moore9Dayle LaPolla10Veronica Fitzpatrick11Maureen Ward12J. David Warren13Claudia Fischbach14Vivek Mittal15Linda T. Vahdat16Memorial Sloan Kettering Cancer CenterNordic Bioscience- ProscionNordic Bioscience- Cancer departmentWeill Cornell MedicineMemorial Sloan Kettering Cancer CenterNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell UniversityWeill Cornell MedicineWeill Cornell MedicineWeill Cornell MedicineWeill Cornell MedicineWeill Cornell MedicineMemorial Sloan Kettering Cancer CenterWeill Cornell MedicineWeill Cornell MedicineNancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell UniversityWeill Cornell MedicineMemorial Sloan Kettering Cancer CenterAbstract 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.https://doi.org/10.1038/s41523-021-00313-w
collection DOAJ
language English
format Article
sources DOAJ
author Ying L. Liu
Cecilie Liv Bager
Nicholas Willumsen
Divya Ramchandani
Naomi Kornhauser
Lu Ling
Marta Cobham
Eleni Andreopoulou
Tessa Cigler
Anne Moore
Dayle LaPolla
Veronica Fitzpatrick
Maureen Ward
J. David Warren
Claudia Fischbach
Vivek Mittal
Linda T. Vahdat
spellingShingle Ying L. Liu
Cecilie Liv Bager
Nicholas Willumsen
Divya Ramchandani
Naomi Kornhauser
Lu Ling
Marta Cobham
Eleni Andreopoulou
Tessa Cigler
Anne Moore
Dayle LaPolla
Veronica Fitzpatrick
Maureen Ward
J. David Warren
Claudia Fischbach
Vivek Mittal
Linda T. Vahdat
Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
npj Breast Cancer
author_facet Ying L. Liu
Cecilie Liv Bager
Nicholas Willumsen
Divya Ramchandani
Naomi Kornhauser
Lu Ling
Marta Cobham
Eleni Andreopoulou
Tessa Cigler
Anne Moore
Dayle LaPolla
Veronica Fitzpatrick
Maureen Ward
J. David Warren
Claudia Fischbach
Vivek Mittal
Linda T. Vahdat
author_sort Ying L. Liu
title Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
title_short Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
title_full Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
title_fullStr Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
title_full_unstemmed Tetrathiomolybdate (TM)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
title_sort tetrathiomolybdate (tm)-associated copper depletion influences collagen remodeling and immune response in the pre-metastatic niche of breast cancer
publisher Nature Publishing Group
series npj Breast Cancer
issn 2374-4677
publishDate 2021-08-01
description 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.
url https://doi.org/10.1038/s41523-021-00313-w
work_keys_str_mv AT yinglliu tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT cecilielivbager tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT nicholaswillumsen tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT divyaramchandani tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT naomikornhauser tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT luling tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT martacobham tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT eleniandreopoulou tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT tessacigler tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT annemoore tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT daylelapolla tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT veronicafitzpatrick tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT maureenward tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT jdavidwarren tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT claudiafischbach tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT vivekmittal tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
AT lindatvahdat tetrathiomolybdatetmassociatedcopperdepletioninfluencescollagenremodelingandimmuneresponseinthepremetastaticnicheofbreastcancer
_version_ 1721186684292300800