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Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling

Biophysical cues of rigid tumor matrix play a critical role in cancer cell malignancy. We report that stiffly confined cancer cells exhibit robust growth of spheroids in the stiff hydrogel that exerts substantial confining stress on the cells. The stressed condition activated Hsp (heat shock protein...

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Autores principales: Wong, Siu Hong Dexter, Yin, Bohan, Li, Zhuo, Yuan, Weihao, Zhang, Qin, Xie, Xian, Tan, Youhua, Wong, Nathalie, Zhang, Kunyu, Bian, Liming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328411/
https://www.ncbi.nlm.nih.gov/pubmed/37418519
http://dx.doi.org/10.1126/sciadv.adg9593
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author Wong, Siu Hong Dexter
Yin, Bohan
Li, Zhuo
Yuan, Weihao
Zhang, Qin
Xie, Xian
Tan, Youhua
Wong, Nathalie
Zhang, Kunyu
Bian, Liming
author_facet Wong, Siu Hong Dexter
Yin, Bohan
Li, Zhuo
Yuan, Weihao
Zhang, Qin
Xie, Xian
Tan, Youhua
Wong, Nathalie
Zhang, Kunyu
Bian, Liming
author_sort Wong, Siu Hong Dexter
collection PubMed
description Biophysical cues of rigid tumor matrix play a critical role in cancer cell malignancy. We report that stiffly confined cancer cells exhibit robust growth of spheroids in the stiff hydrogel that exerts substantial confining stress on the cells. The stressed condition activated Hsp (heat shock protein)–signal transducer and activator of transcription 3 signaling via the transient receptor potential vanilloid 4–phosphatidylinositol 3-kinase/Akt axis, thereby up-regulating the expression of the stemness-related markers in cancer cells, whereas these signaling activities were suppressed in cancer cells cultured in softer hydrogels or stiff hydrogels with stress relief or Hsp70 knockdown/inhibition. This mechanopriming based on three-dimensional culture enhanced cancer cell tumorigenicity and metastasis in animal models upon transplantation, and pharmaceutically inhibiting Hsp70 improved the anticancer efficacy of chemotherapy. Mechanistically, our study reveals the crucial role of Hsp70 in regulating cancer cell malignancy under mechanically stressed conditions and its impacts on cancer prognosis–related molecular pathways for cancer treatments.
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spelling pubmed-103284112023-07-08 Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling Wong, Siu Hong Dexter Yin, Bohan Li, Zhuo Yuan, Weihao Zhang, Qin Xie, Xian Tan, Youhua Wong, Nathalie Zhang, Kunyu Bian, Liming Sci Adv Biomedicine and Life Sciences Biophysical cues of rigid tumor matrix play a critical role in cancer cell malignancy. We report that stiffly confined cancer cells exhibit robust growth of spheroids in the stiff hydrogel that exerts substantial confining stress on the cells. The stressed condition activated Hsp (heat shock protein)–signal transducer and activator of transcription 3 signaling via the transient receptor potential vanilloid 4–phosphatidylinositol 3-kinase/Akt axis, thereby up-regulating the expression of the stemness-related markers in cancer cells, whereas these signaling activities were suppressed in cancer cells cultured in softer hydrogels or stiff hydrogels with stress relief or Hsp70 knockdown/inhibition. This mechanopriming based on three-dimensional culture enhanced cancer cell tumorigenicity and metastasis in animal models upon transplantation, and pharmaceutically inhibiting Hsp70 improved the anticancer efficacy of chemotherapy. Mechanistically, our study reveals the crucial role of Hsp70 in regulating cancer cell malignancy under mechanically stressed conditions and its impacts on cancer prognosis–related molecular pathways for cancer treatments. American Association for the Advancement of Science 2023-07-07 /pmc/articles/PMC10328411/ /pubmed/37418519 http://dx.doi.org/10.1126/sciadv.adg9593 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Wong, Siu Hong Dexter
Yin, Bohan
Li, Zhuo
Yuan, Weihao
Zhang, Qin
Xie, Xian
Tan, Youhua
Wong, Nathalie
Zhang, Kunyu
Bian, Liming
Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title_full Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title_fullStr Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title_full_unstemmed Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title_short Mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
title_sort mechanical manipulation of cancer cell tumorigenicity via heat shock protein signaling
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328411/
https://www.ncbi.nlm.nih.gov/pubmed/37418519
http://dx.doi.org/10.1126/sciadv.adg9593
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