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典型文献
Epigenetic reprogramming in small cell lung cancer
文献摘要:
Small cell lung cancer (SCLC), a highly lethal lung cancer sub-type with distinct neuroendocrine-like features, accounts for 10%–15% of all lung cancers. The overall 5-year survival rate remains less than 10%. SCLC is characterized by early metastasis, thus minimizing the potential patient benefits of surgery. In recent decades, the first-line treatment for SCLC has remained chemotherapy combining etoposide and cis-platin (E/P). Despite high rates of response to E/P treatment, SCLC eventually relapses and is almost universally resistant to treatment at recurrence, thus making SCLC a recalcitrant malignancy. Moreover, the limited knowledge regarding the molecular mechanisms underlying SCLC metastasis and resistance greatly hinders improvements in overall SCLC survival. To better understand the molecular mechanisms of SCLC and discover potential therapeutic targets, extensive efforts have continued for decades. Recently, several studies have implicated epigenetic modifications, including histone modifications, DNA methylation, and chromatin accessibil-ity, in SCLC. NFIB has been documented to promote SCLC metastasis through a widespread increase in chromatin acces-sibility1. Of particular note, one recent study has indicated that KMT2C deficiency promotes SCLC metastasis through DNMT3A-mediated epigenetic reprogramming involving both histone and DNA hypomethylation2. These studies have revealed that epigenetic reprogramming plays an impor-tant role in SCLC. In this review, we summarize and discuss the advances in basic and translational research in SCLC, which have revealed the functional and targetable roles of epigenetic modifications during tumorigenesis, metastasis, and chemoresistance.
文献关键词:
作者姓名:
Jingyao Chen;Xiangyu Pan;Feifei Na;Xuelan Chen;Chong Chen
作者机构:
State Key Laboratory of Biotherapy and Cancer Center,West China Hospital,Sichuan University,Chengdu 610044,China;Department of Thoracic Oncology,West China Hospital,Sichuan University,Chengdu 610044,China
引用格式:
[1]Jingyao Chen;Xiangyu Pan;Feifei Na;Xuelan Chen;Chong Chen-.Epigenetic reprogramming in small cell lung cancer)[J].癌症生物学与医学(英文版),2022(08):1111-1116
A类:
platin,accessibil,sibility1,hypomethylation2,targetable
B类:
Epigenetic,reprogramming,small,cell,lung,Small,SCLC,highly,lethal,sub,type,distinct,neuroendocrine,like,features,accounts,cancers,overall,year,survival,remains,less,than,characterized,by,early,metastasis,thus,minimizing,potential,patient,benefits,surgery,In,recent,decades,first,line,treatment,has,remained,chemotherapy,combining,etoposide,cis,Despite,rates,response,eventually,relapses,almost,universally,resistant,recurrence,making,recalcitrant,malignancy,Moreover,limited,knowledge,regarding,molecular,mechanisms,underlying,greatly,hinders,improvements,To,better,understand,discover,therapeutic,targets,extensive,efforts,have,continued,Recently,several,studies,implicated,epigenetic,modifications,including,histone,chromatin,NFIB,been,documented,through,widespread,increase,Of,particular,note,study,indicated,that,KMT2C,deficiency,promotes,DNMT3A,mediated,involving,both,These,revealed,plays,impor,this,review,we,summarize,discuss,advances,basic,translational,research,which,functional,roles,nbsp,during,tumorigenesis,chemoresistance
AB值:
0.579038
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