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机构地区:[1]Institute for Clinical and Translational Research,Baylor College of Medicine,Houston,Texas,USA [2]Section of Epidemiology and Population Sciences,Department of Medicine,Baylor College of Medicine,Houston,Texas,USA [3]Dan L Duncan Comprehensive Cancer Center,Baylor College of Medicine,Houston,Texas,USA
出 处:《Cancer Communications》2024年第5期589-592,共4页癌症通讯(英文)
基 金:supported by the Cancer Prevention Research Institute of Texas(CPRIT)(RR180061 to CC);the National Cancer Institute of the National Institute of Health(1R01CA269764 to CC).CC is a CPRIT Scholar in Cancer Research.
摘 要:Infiltrating immune cells in the tumor microenvironment(TME)play critical roles in the initiation,progression,and metastasis of cancer[1].Previous studies have reported that the infiltration levels of various immune cell types are significantly associated with patient prognosis in different cancers[2,3].Specifically,in non-small cell lung cancer(NSCLC)the prognostic associations of major immune cell types have been investigated[4–6],however,some of the reported associations are inconsistent and remain debated[7].Limited by technical issues,most studies focused on a few immune cell lineages or relied on inferred immune cell levels from computational deconvolution.To investigate the prognostic effects of all major immune cell types unbiasedly,more systematic high-quality immune cell profiling data with matched patient survival information are needed.
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