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Cited by 537

The DOI matches its Crossref record; 150 of the 150 references it cites were found in a registry or an index.

Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy

Open access
Krug, Karsten, Jaehnig, Eric J., Satpathy, Shankha, Blumenberg, Lili, Karpova, Alla, Anurag, Meenakshi, Miles, George, Mertins, Philipp, Geffen, Yifat, Tang, Lauren C., Heiman, David I., Cao, Song, Maruvka, Yosef E., Lei, Jonathan T., Huang, Chen, Kothadia, Ramani B., Colaprico, Antonio, Birger, Chet, Wang, Jarey, Dou, Yongchao, Wen, Bo, Shi, Zhiao, Liao, Yuxing, Wiznerowicz, Maciej, Wyczalkowski, Matthew A., Chen, Xi Steven, Kennedy, Jacob J., Paulovich, Amanda G., Thiagarajan, Mathangi, Kinsinger, Christopher R., Hiltke, Tara, Boja, Emily S., Mesri, Mehdi, Robles, Ana I., Rodriguez, Henry, Westbrook, Thomas F., Ding, Li, Getz, Gad, Clauser, Karl R., Fenyö, David, Ruggles, Kelly V., Zhang, Bing, Mani, D.R., Carr, Steven A., Ellis, Matthew J., Gillette, Michael A., Avanessian, Shayan C., Cai, Shuang, Chan, Daniel, Chen, Xian, Edwards, Nathan J., Hoofnagle, Andrew N., Kane, M. Harry, Ketchum, Karen A., Kuhn, Eric, Levine, Douglas A., Li, Shunqiang, Liebler, Daniel C., Liu, Tao, Luo, Jingqin, Madhavan, Subha, Maher, Chris, McDermott, Jason E., McGarvey, Peter B., Oberti, Mauricio, Pandey, Akhilesh, Payne, Samuel H., Ransohoff, David F., Rivers, Robert C., Rodland, Karin D., Rudnick, Paul, Sanders, Melinda E., Shaw, Kenna M., Shih, Ie-Ming, Slebos, Robbert J.C., Smith, Richard D., Snyder, Michael, Stein, Stephen E., Tabb, David L., Thangudu, Ratna R., Thomas, Stefani, Wang, Yue, White, Forest M., Whiteaker, Jeffrey R., Whiteley, Gordon A., Zhang, Hui, Zhang, Zhen, Zhao, Yingming, Zhu, Heng, Zimmerman, Lisa J.·2020·Cell

Abstract

The integration of mass spectrometry-based proteomics with next-generation DNA and RNA sequencing profiles tumors more comprehensively. Here this "proteogenomics" approach was applied to 122 treatment-naive primary breast cancers accrued to preserve post-translational modifications, including protein phosphorylation and acetylation. Proteogenomics challenged standard breast cancer diagnoses, provided detailed analysis of the ERBB2 amplicon, defined tumor subsets that could benefit from immune checkpoint therapy, and allowed more accurate assessment of Rb status for prediction of CDK4/6 inhibitor responsiveness. Phosphoproteomics profiles uncovered novel associations between tumor suppressor loss and targetable kinases. Acetylproteome analysis highlighted acetylation on key nuclear proteins involved in the DNA damage response and revealed cross-talk between cytoplasmic and mitochondrial acetylation and metabolism. Our results underscore the potential of proteogenomics for clinical investigation of breast cancer through more accurate annotation of targetable pathways and biological features of this remarkably heterogeneous malignancy.

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Authors
Krug, K., Jaehnig, E. J., Satpathy, S., Blumenberg, L., Karpova, A., Anurag, M., Miles, G., Mertins, P., Geffen, Y., Tang, L. C., Heiman, D. I., Cao, S., Maruvka, Y. E., Lei, J. T., Huang, C., Kothadia, R. B., Colaprico, A., Birger, C., Wang, J., Dou, Y., Wen, B., Shi, Z., Liao, Y., Wiznerowicz, M., Wyczalkowski, M. A., Chen, X. S., Kennedy, J. J., Paulovich, A. G., Thiagarajan, M., Kinsinger, C. R., Hiltke, T., Boja, E. S., Mesri, M., Robles, A. I., Rodriguez, H., Westbrook, T. F., Ding, L., Getz, G., Clauser, K. R., Fenyö, D., Ruggles, K. V., Zhang, B., Mani, D. R., Carr, S. A., Ellis, M. J., Gillette, M. A., Avanessian, S. C., Cai, S., Chan, D., Chen, X., Edwards, N. J., Hoofnagle, A. N., Kane, M. H., Ketchum, K. A., Kuhn, E., Levine, D. A., Li, S., Liebler, D. C., Liu, T., Luo, J., Madhavan, S., Maher, C., McDermott, J. E., McGarvey, P. B., Oberti, M., Pandey, A., Payne, S. H., Ransohoff, D. F., Rivers, R. C., Rodland, K. D., Rudnick, P., Sanders, M. E., Shaw, K. M., Shih, I.-M., Slebos, R. J. C., Smith, R. D., Snyder, M., Stein, S. E., Tabb, D. L., Thangudu, R. R., Thomas, S., Wang, Y., White, F. M., Whiteaker, J. R., Whiteley, G. A., Zhang, H., Zhang, Z., Zhao, Y., Zhu, H., & Zimmerman, L. J.
Venue
Cell
Publisher
Elsevier BV
Published
2020-11
Volume
183
Issue
5
Pages
1436-1456.e31
ISSN
0092-8674 (ISSN-L)
OpenAlex
W3104755560
Cited by
537
References
150
FWCI
23.34
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy. https://app.cochat.ai/papers/10.1016/j.cell.2020.10.036
The paper
Krug, K., Jaehnig, E. J., Satpathy, S., Blumenberg, L., Karpova, A., Anurag, M., Miles, G., Mertins, P., Geffen, Y., Tang, L. C., Heiman, D. I., Cao, S., Maruvka, Y. E., Lei, J. T., Huang, C., Kothadia, R. B., Colaprico, A., Birger, C., Wang, J., . . . Zimmerman, L. J. (2020). Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy. Cell. https://doi.org/10.1016/j.cell.2020.10.036

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.