Integrating proteomics into precision oncology

被引:17
|
作者
Wahjudi, Leonie W. [1 ]
Bernhardt, Stephan [1 ]
Abnaof, Khalid [1 ]
Horak, Peter [2 ,3 ,4 ]
Kreutzfeldt, Simon [2 ,3 ,4 ]
Heining, Christoph [5 ,7 ,8 ,9 ]
Borgoni, Simone [1 ,10 ]
Becki, Corinna [1 ]
Berg, Daniela [1 ]
Richter, Daniela [5 ,7 ]
Hutter, Barbara [4 ,11 ,12 ]
Uhrig, Sebastian [4 ,10 ,11 ,12 ]
Pfuetze, Katrin [2 ,3 ,4 ]
Leichsenring, Jonas [13 ]
Glimm, Hanno [3 ,5 ,6 ,7 ,8 ,9 ]
Brors, Benedikt [4 ,11 ,12 ]
von Kalle, Christof [2 ,3 ,6 ]
Stenzinger, Albrecht [4 ,13 ]
Korf, Ulrike [1 ]
Froehling, Stefan [2 ,3 ,4 ]
Wiemann, Stefan [1 ,4 ]
机构
[1] German Canc Res Ctr, Div Mol Genome Anal, Heidelberg, Germany
[2] Natl Ctr Tumor Dis NCT Heidelberg, Div Translat Med Oncol, Neuenheimer Feld 460, D-69120 Heidelberg, Germany
[3] German Canc Res Ctr, Neuenheimer Feld 460, D-69120 Heidelberg, Germany
[4] German Canc Consortium DKTK, Heidelberg, Germany
[5] Natl Ctr Tumor Dis NCT Dresden, Dept Translat Med Oncol, Dresden, Germany
[6] Natl Ctr Tumor Dis NCT, Translat Funct Canc Genom, Heidelberg, Germany
[7] German Canc Consortium DKTK, Dresden, Germany
[8] Tech Univ Dresden, Ctr Personalized Oncol, Natl Ctr Tumour Dis NCT Dresden, Dresden, Germany
[9] Tech Univ Dresden, Univ Hosp Carl Gustav Carus Dresden, Dresden, Germany
[10] Heidelberg Univ, Fac Biosci, Heidelberg, Germany
[11] German Canc Res Ctr, Div Appl Bioinformat, Heidelberg, Germany
[12] Natl Ctr Tumor Dis NCT Heidelberg, Heidelberg, Germany
[13] Heidelberg Univ, Inst Pathol, Heidelberg, Germany
关键词
genomics; precision oncology; proteomics; therapeutic decision making; HOMOLOGOUS RECOMBINATION; BIOMARKER DISCOVERY; CANCER; INHIBITION; DEFICIENCY; ACTIVATION; VARIANTS; TARGETS; ARRAYS; ERA;
D O I
10.1002/ijc.33301
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA sequencing and RNA sequencing are increasingly applied in precision oncology, where molecular tumor boards evaluate the actionability of genetic events in individual tumors to guide targeted treatment. To work toward an additional level of patient characterization, we assessed the abundance and activity of 27 proteins in 134 patients whose tumors had previously undergone whole-exome and RNA sequencing within the Molecularly Aided Stratification for Tumor Eradication Research (MASTER) program of National Center for Tumor Diseases, Heidelberg. Proteomic and phosphoproteomic targets were selected to reflect the most relevant therapeutic baskets in MASTER. Among six different therapeutic baskets, the proteomic data supported treatment recommendations that were based on DNA and RNA analyses in 10% to 57% and frequently suggested alternative treatment options. In several cases, protein activities explained the patients' clinical course and provided potential explanations for treatment failure. Our study indicates that the integrative analysis of DNA, RNA and protein data may refine therapeutic stratification of individual patients and, thus, holds potential to increase the success rate of precision cancer therapy. Prospective validation studies are needed to advance the integration of proteomic analysis into precision oncology.
引用
收藏
页码:1438 / 1451
页数:14
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