Serum Metabolic Profile Alteration Reveals Response to Platinum-Based Combination Chemotherapy for Lung Cancer: Sensitive Patients Distinguished from Insensitive ones.
Serum Metabolic Profile Alteration Reveals Response to Platinum-Based Combination Chemotherapy for Lung Cancer: Sensitive Patients Distinguished from Insensitive ones.
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血清代谢谱的改变揭示了对肺癌铂类联合化疗的反应:敏感患者与不敏感患者的区别
DOI:
10.1038/s41598-017-16085-y
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发表时间:
2017-12-13
影响因子:
4.6
通讯作者:
Cui Y
中科院分区:
文献类型:
--
作者:
Xu S;Zhou Y;Geng H;Song D;Tang J;Zhu X;Yu D;Hu S;Cui Y
Most lung cancers are diagnosed at fairly advanced stages due to limited clinical symptoms. Platinum-based chemotherapy, either as single regimen or in combination with radiation, is one of the major recommendations for the patients. Earlier evaluation of the effectiveness of the chemotherapies is critical for developing better treatment plan given the toxicity of the chemotherapeutic reagents. Drug efficacy could be reflected in the systemic metabolism characteristics though knowledge about which remains scarce. In this study, serum metabolism influence of three types of commonly used platinum-based combination chemotherapy regimens, namely cisplatin with gemcitabine, vinorelbine or docetaxel, were studied using pattern recognition coupled with nuclear magnetic resonance techniques. The treated patients were divided into sensitive or insensitive subgroups according to their response to the treatments. We found that insensitive subjects can be identified from the sensitive ones with up-regulation of glucose and taurine but reduced alanine and lactate concentrations in serum. The combination chemotherapy of lung cancer is accompanied by disturbances of multiple metabolic pathways such as energy metabolism, phosphatidylcholine biosynthesis, so that the treated patients were marginally discriminated from the untreated. Serum metabolic profile of patients shows potential as an indicator of their response to platinum-based combination chemotherapy.
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影响因子:
3.7
作者:
Lodi A;Ronen SM
通讯作者:
Ronen SM
DOI:
10.1056/nejmoa1214271
发表时间:
2013-03-21
期刊:
The New England journal of medicine
影响因子:
--
作者:
Friboulet L;Olaussen KA;Pignon JP;Shepherd FA;Tsao MS;Graziano S;Kratzke R;Douillard JY;Seymour L;Pirker R;Filipits M;André F;Solary E;Ponsonnailles F;Robin A;Stoclin A;Dorvault N;Commo F;Adam J;Vanhecke E;Saulnier P;Thomale J;Le Chevalier T;Dunant A;Rousseau V;Le Teuff G;Brambilla E;Soria JC
通讯作者:
Soria JC
影响因子:
9.7
作者:
Jobard, Elodie;Pontoizeau, Clement;Tredan, Olivier
通讯作者:
Tredan, Olivier
影响因子:
13.5
作者:
Guo, Weijie;Qiu, Zhaoping;He, Xianghuo
通讯作者:
He, Xianghuo
DOI:
10.1016/j.chemolab.2014.04.014
发表时间:
2014-07-15
影响因子:
3.9
作者:
Li, Ya-Qiong;Liu, Yi-Fei;Cui, Yan-Fang
通讯作者:
Cui, Yan-Fang