YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation
The oncogene YAP has been shown previously to promote tumor growth and metastasis. However, how YAP influences the behavior of tumor cells traveling within the circulatory system has not been as well explored. Given that rate-limiting steps of metastasis are known to occur while tumor cells enter, t...
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American Association for Cancer Research (AACR)
2021
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Online Access: | https://hdl.handle.net/1721.1/133297 |
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author | Benjamin, David C Kang, Joon Ho Hamza, Bashar King, Emily M Lamar, John M Manalis, Scott R Hynes, Richard O |
author2 | Massachusetts Institute of Technology. Department of Biology |
author_facet | Massachusetts Institute of Technology. Department of Biology Benjamin, David C Kang, Joon Ho Hamza, Bashar King, Emily M Lamar, John M Manalis, Scott R Hynes, Richard O |
author_sort | Benjamin, David C |
collection | MIT |
description | The oncogene YAP has been shown previously to promote tumor growth and metastasis. However, how YAP influences the behavior of tumor cells traveling within the circulatory system has not been as well explored. Given that rate-limiting steps of metastasis are known to occur while tumor cells enter, travel through, or exit circulation, we sought to study how YAP influences tumor cell behavior within the circulatory system. Intravital imaging in live zebrafish embryos revealed that YAP influenced the distribution of tumor cells within the animal following intravenous injection. Control cells became lodged in the first capillary bed encountered in the tail, whereas cells overexpressing constitutively active YAP were able to travel through this capillary plexus, reenter systemic circulation, and seed in the brain. YAP controlled transit through these capillaries by promoting active migration within the vasculature. These results were corroborated in a mouse model following intravenous injection, where active YAP increased the number of circulating tumor cells over time. Our results suggest a possible mechanism whereby tumor cells can spread to organs beyond the first capillary bed downstream from the primary tumor. These results also show that a specific gene can affect the distribution of tumor cells within an animal, thereby influencing the global pattern of metastasis in that animal. |
first_indexed | 2024-09-23T13:53:24Z |
format | Article |
id | mit-1721.1/133297 |
institution | Massachusetts Institute of Technology |
language | English |
last_indexed | 2024-09-23T13:53:24Z |
publishDate | 2021 |
publisher | American Association for Cancer Research (AACR) |
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spelling | mit-1721.1/1332972023-09-12T20:12:50Z YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation Benjamin, David C Kang, Joon Ho Hamza, Bashar King, Emily M Lamar, John M Manalis, Scott R Hynes, Richard O Massachusetts Institute of Technology. Department of Biology Koch Institute for Integrative Cancer Research at MIT Howard Hughes Medical Institute Massachusetts Institute of Technology. Department of Physics Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Mechanical Engineering The oncogene YAP has been shown previously to promote tumor growth and metastasis. However, how YAP influences the behavior of tumor cells traveling within the circulatory system has not been as well explored. Given that rate-limiting steps of metastasis are known to occur while tumor cells enter, travel through, or exit circulation, we sought to study how YAP influences tumor cell behavior within the circulatory system. Intravital imaging in live zebrafish embryos revealed that YAP influenced the distribution of tumor cells within the animal following intravenous injection. Control cells became lodged in the first capillary bed encountered in the tail, whereas cells overexpressing constitutively active YAP were able to travel through this capillary plexus, reenter systemic circulation, and seed in the brain. YAP controlled transit through these capillaries by promoting active migration within the vasculature. These results were corroborated in a mouse model following intravenous injection, where active YAP increased the number of circulating tumor cells over time. Our results suggest a possible mechanism whereby tumor cells can spread to organs beyond the first capillary bed downstream from the primary tumor. These results also show that a specific gene can affect the distribution of tumor cells within an animal, thereby influencing the global pattern of metastasis in that animal. 2021-10-27T19:51:59Z 2021-10-27T19:51:59Z 2020 2021-07-16T17:14:08Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/133297 en 10.1158/0008-5472.CAN-20-0212 Cancer Research Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf American Association for Cancer Research (AACR) PMC |
spellingShingle | Benjamin, David C Kang, Joon Ho Hamza, Bashar King, Emily M Lamar, John M Manalis, Scott R Hynes, Richard O YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title | YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title_full | YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title_fullStr | YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title_full_unstemmed | YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title_short | YAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation |
title_sort | yap enhances tumor cell dissemination by promoting intravascular motility and reentry into systemic circulation |
url | https://hdl.handle.net/1721.1/133297 |
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