Measuring competitive exclusion in non-small cell lung cancer

被引:26
作者
Farrokhian, Nathan [1 ]
Maltas, Jeff [2 ]
Dinh, Mina [2 ]
Durmaz, Arda [1 ]
Ellsworth, Patrick [1 ]
Hitomi, Masahiro [2 ]
McClure, Erin [2 ]
Marusyk, Andriy [3 ]
Kaznatcheev, Artem [4 ]
Scott, Jacob G. [1 ,2 ,5 ]
机构
[1] CWRU Sch Med, Cleveland, OH 44106 USA
[2] Cleveland Clin, Dept Translat Hematol & Oncol Res, Cleveland, OH 44106 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Canc Physiol, Tampa, FL USA
[4] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[5] Cleveland Clin, Dept Radiat Oncol, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
INTRATUMOR HETEROGENEITY; INHIBITOR GEFITINIB; MUTATOR PHENOTYPE; EVOLUTION; RESISTANCE; COOPERATION; EXPRESSION; GAMES; HEAD;
D O I
10.1126/sciadv.abm7212
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, we experimentally measure the frequency-dependent interactions between a gefitinib-resistant non-small cell lung cancer population and its sensitive ancestor via the evolutionary game assay. We show that cost of resistance is insufficient to accurately predict competitive exclusion and that frequency-dependent growth rate measurements are required. Using frequency-dependent growth rate data, we then show that gefitinib treatment results in competitive exclusion of the ancestor, while the absence of treatment results in a likely, but not guaranteed, exclusion of the resistant strain. Then, using simulations, we demonstrate that incorporating ecological growth effects can influence the predicted extinction time. In addition, we show that higher drug concentrations may not lead to the optimal reduction in tumor burden. Together, these results highlight the potential importance of frequency-dependent growth rate data for understanding competing populations, both in the laboratory and as we translate adaptive therapy regimens to the clinic.
引用
收藏
页数:10
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