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Merck

Proteogenomic Characterization of Endometrial Carcinoma.

Cell (2020-02-16)
Yongchao Dou, Emily A Kawaler, Daniel Cui Zhou, Marina A Gritsenko, Chen Huang, Lili Blumenberg, Alla Karpova, Vladislav A Petyuk, Sara R Savage, Shankha Satpathy, Wenke Liu, Yige Wu, Chia-Feng Tsai, Bo Wen, Zhi Li, Song Cao, Jamie Moon, Zhiao Shi, MacIntosh Cornwell, Matthew A Wyczalkowski, Rosalie K Chu, Suhas Vasaikar, Hua Zhou, Qingsong Gao, Ronald J Moore, Kai Li, Sunantha Sethuraman, Matthew E Monroe, Rui Zhao, David Heiman, Karsten Krug, Karl Clauser, Ramani Kothadia, Yosef Maruvka, Alexander R Pico, Amanda E Oliphant, Emily L Hoskins, Samuel L Pugh, Sean J I Beecroft, David W Adams, Jonathan C Jarman, Andy Kong, Hui-Yin Chang, Boris Reva, Yuxing Liao, Dmitry Rykunov, Antonio Colaprico, Xi Steven Chen, Andrzej Czekański, Marcin Jędryka, Rafał Matkowski, Maciej Wiznerowicz, Tara Hiltke, Emily Boja, Christopher R Kinsinger, Mehdi Mesri, Ana I Robles, Henry Rodriguez, David Mutch, Katherine Fuh, Matthew J Ellis, Deborah DeLair, Mathangi Thiagarajan, D R Mani, Gad Getz, Michael Noble, Alexey I Nesvizhskii, Pei Wang, Matthew L Anderson, Douglas A Levine, Richard D Smith, Samuel H Payne, Kelly V Ruggles, Karin D Rodland, Li Ding, Bing Zhang, Tao Liu, David Fenyö
摘要

We undertook a comprehensive proteogenomic characterization of 95 prospectively collected endometrial carcinomas, comprising 83 endometrioid and 12 serous tumors. This analysis revealed possible new consequences of perturbations to the p53 and Wnt/β-catenin pathways, identified a potential role for circRNAs in the epithelial-mesenchymal transition, and provided new information about proteomic markers of clinical and genomic tumor subgroups, including relationships to known druggable pathways. An extensive genome-wide acetylation survey yielded insights into regulatory mechanisms linking Wnt signaling and histone acetylation. We also characterized aspects of the tumor immune landscape, including immunogenic alterations, neoantigens, common cancer/testis antigens, and the immune microenvironment, all of which can inform immunotherapy decisions. Collectively, our multi-omic analyses provide a valuable resource for researchers and clinicians, identify new molecular associations of potential mechanistic significance in the development of endometrial cancers, and suggest novel approaches for identifying potential therapeutic targets.

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Sigma-Aldrich
甲酸, puriss. p.a., ACS reagent, reag. Ph. Eur., ≥98%
Sigma-Aldrich
氯化钙, anhydrous, granular, ≤7.0 mm, ≥93.0%
Sigma-Aldrich
磷酸酶抑制剂混合物2, aqueous solution (dark coloration may develop upon storage, which does not affect the activity)
Sigma-Aldrich
苯甲磺酰氟 溶液, ~0.1 M in ethanol (T)
Sigma-Aldrich
氯化钠, BioXtra, ≥99.5% (AT)
Sigma-Aldrich
乙二胺四乙酸 二钠盐 溶液, for molecular biology, 0.5 M in H2O, DNase, RNase, NICKase and protease, none detected
Sigma-Aldrich
PUGNAc, ≥95% (HPLC)
Sigma-Aldrich
Nα-乙酰基-L-赖氨酸