The Dormancy Dilemma: Quiescence versus Balanced Proliferation

Metastatic dissemination with subsequent clinical outgrowth leads to the greatest part of morbidity and mortality from most solid tumors. Even more daunting is that many of these metastatic deposits silently lie undetected, recurring years to decades after primary tumor extirpation by surgery or rad...

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Main Authors: Wells, Alan, Griffith, Linda G., Wells, Jakob Z., Taylor, Donald P.
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: American Association for Cancer Research 2015
Online Access:http://hdl.handle.net/1721.1/99378
https://orcid.org/0000-0002-1801-5548
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author Wells, Alan
Griffith, Linda G.
Wells, Jakob Z.
Taylor, Donald P.
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Wells, Alan
Griffith, Linda G.
Wells, Jakob Z.
Taylor, Donald P.
author_sort Wells, Alan
collection MIT
description Metastatic dissemination with subsequent clinical outgrowth leads to the greatest part of morbidity and mortality from most solid tumors. Even more daunting is that many of these metastatic deposits silently lie undetected, recurring years to decades after primary tumor extirpation by surgery or radiation (termed metastatic dormancy). As primary tumors are frequently curable, a critical focus now turns to preventing the lethal emergence from metastatic dormancy. Current carcinoma treatments include adjuvant therapy intended to kill the cryptic metastatic tumor cells. Because such standard therapies mainly kill cycling cells, this approach carries an implicit assumption that metastatic cells are in the mitogenic cycle. Thus, the pivotal question arises as to whether clinically occult micrometastases survive in a state of balanced proliferation and death, or whether these cells undergo at least long periods of quiescence marked by cell-cycle arrest. The treatment implications are thus obvious—if the carcinoma cells are cycling then therapies should target cycling cells, whereas if cells are quiescent then therapies should either maintain dormancy or be toxic to dormant cells. Because this distinction is paramount to rational therapeutic development and administration, we investigated whether quiescence or balanced proliferation is the most likely etiology underlying metastatic dormancy. We recently published a computer simulation study that determined that balanced proliferation is not the likely driving force and that quiescence most likely participates in metastatic dormancy. As such, a greater emphasis on developing diagnostics and therapeutics for quiescent carcinomas is needed.
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spelling mit-1721.1/993782022-09-30T11:22:12Z The Dormancy Dilemma: Quiescence versus Balanced Proliferation Wells, Alan Griffith, Linda G. Wells, Jakob Z. Taylor, Donald P. Massachusetts Institute of Technology. Department of Biological Engineering Griffith, Linda G. Metastatic dissemination with subsequent clinical outgrowth leads to the greatest part of morbidity and mortality from most solid tumors. Even more daunting is that many of these metastatic deposits silently lie undetected, recurring years to decades after primary tumor extirpation by surgery or radiation (termed metastatic dormancy). As primary tumors are frequently curable, a critical focus now turns to preventing the lethal emergence from metastatic dormancy. Current carcinoma treatments include adjuvant therapy intended to kill the cryptic metastatic tumor cells. Because such standard therapies mainly kill cycling cells, this approach carries an implicit assumption that metastatic cells are in the mitogenic cycle. Thus, the pivotal question arises as to whether clinically occult micrometastases survive in a state of balanced proliferation and death, or whether these cells undergo at least long periods of quiescence marked by cell-cycle arrest. The treatment implications are thus obvious—if the carcinoma cells are cycling then therapies should target cycling cells, whereas if cells are quiescent then therapies should either maintain dormancy or be toxic to dormant cells. Because this distinction is paramount to rational therapeutic development and administration, we investigated whether quiescence or balanced proliferation is the most likely etiology underlying metastatic dormancy. We recently published a computer simulation study that determined that balanced proliferation is not the likely driving force and that quiescence most likely participates in metastatic dormancy. As such, a greater emphasis on developing diagnostics and therapeutics for quiescent carcinomas is needed. National Institutes of Health (U.S.). National Center for Advancing Translational Sciences (Grant UH2TR000496) 2015-10-20T20:01:47Z 2015-10-20T20:01:47Z 2013-06 2013-03 Article http://purl.org/eprint/type/JournalArticle 0008-5472 1538-7445 http://hdl.handle.net/1721.1/99378 Wells, A., L. Griffith, J. Z. Wells, and D. P. Taylor. “The Dormancy Dilemma: Quiescence Versus Balanced Proliferation.” Cancer Research 73, no. 13 (June 21, 2013): 3811–3816. https://orcid.org/0000-0002-1801-5548 en_US http://dx.doi.org/10.1158/0008-5472.can-13-0356 Cancer Research Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf American Association for Cancer Research PMC
spellingShingle Wells, Alan
Griffith, Linda G.
Wells, Jakob Z.
Taylor, Donald P.
The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title_full The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title_fullStr The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title_full_unstemmed The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title_short The Dormancy Dilemma: Quiescence versus Balanced Proliferation
title_sort dormancy dilemma quiescence versus balanced proliferation
url http://hdl.handle.net/1721.1/99378
https://orcid.org/0000-0002-1801-5548
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