Expression levels of estrogen receptor beta in conjunction with aromatase predict survival in non-small cell lung cancer.
Expression levels of estrogen receptor beta in conjunction with aromatase predict survival in non-small cell lung cancer.
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DOI:
10.1016/j.lungcan.2011.03.009
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发表时间:
2011-11
期刊:
影响因子:
5.3
通讯作者:
Goodglick, Lee
中科院分区:
文献类型:
--
作者:
Mah, Vei;Marquez, Diana;Alavi, Mohammad;Maresh, Erin L.;Zhang, Li;Yoon, Nam;Horvath, Steve;Bagryanova, Lora;Fishbein, Michael C.;Chia, David;Pietras, Richard;Goodglick, Lee
Estrogen signaling pathways may play a significant role in the pathogenesis of non-small cell lung cancers (NSCLC) as evidenced by the expression of aromatase and estrogen receptors (ERα and ERβ) in many of these tumors. Here we examine whether ERα and ERβ levels in conjunction with aromatase define patient groups with respect to survival outcomes and possible treatment regimens. Immunohistochemistry was performed on a high-density tissue microarray with resulting data and clinical information available for 377 patients. Patients were subdivided by gender, age and tumor histology, and survival data was determined using the Cox proportional hazards model and Kaplan-Meier curves. Neither ERα nor ERβ alone were predictors of survival in NSCLC. However, when coupled with aromatase expression, higher ERβ levels predicted worse survival in patients whose tumors expressed higher levels of aromatase. Although this finding was present in patients of both genders, it was especially pronounced in women ≥ 65 years old, where higher expression of both ERβ and aromatase indicated a markedly worse survival rate than that determined by aromatase alone. Conclusion: Expression of ERβ together with aromatase has predictive value for survival in different gender and age subgroups of NSCLC patients. This predictive value is stronger than each individual marker alone. Our results suggest treatment with aromatase inhibitors alone or combined with estrogen receptor modulators may be of benefit in some subpopulations of these patients.
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影响因子:
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Lynch, TJ;Bell, DW;Haber, DA
通讯作者:
Haber, DA
影响因子:
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Mah, Vei;Seligson, David B.;Goodglick, Lee
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Goodglick, Lee
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Korach, KS
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Fried, Linda P.
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通讯作者:
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