Proteome Landscapes of Human Hepatocellular Carcinoma and Intrahepatic Cholangiocarcinoma
Open accessAbstract
Liver cancer is among the top leading causes of cancer mortality worldwide. Particularly, hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (CCA) have been extensively investigated from the aspect of tumor biology. However, a comprehensive and systematic understanding of the molecular characteristics of HCC and CCA remains absent. Here, we characterized the proteome landscapes of HCC and CCA using the data-independent acquisition (DIA) mass spectrometry (MS) method. By comparing the quantitative proteomes of HCC and CCA, we found several differences between the two cancer types. In particular, we found an abnormal lipid metabolism in HCC and activated extracellular matrix-related pathways in CCA. We next developed a three-protein classifier to distinguish CCA from HCC, achieving an area under the curve (AUC) of 0.92, and an accuracy of 90% in an independent validation cohort of 51 patients. The distinct molecular characteristics of HCC and CCA presented in this study provide new insights into the tumor biology of these two major important primary liver cancers. Our findings may help develop more efficient diagnostic approaches and new targeted drug treatments.
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An opposite, pro-oncogenic role for TBX3 has been revealed in other tumor types, such as malignant melanoma, breast, gastric, and cervical cancers.
“An opposite, pro-oncogenic role for TBX3 has been revealed in other tumor types, such as malignant melanoma, breast, gastric, and cervical cancers [1–3].”
From Overexpression of TBX3 suppresses tumorigenesis in experimental and human cholangiocarcinoma (2024) · cites this paper as [3]
The Results and Discussion section examines protein expression in hepatocellular carcinoma and cholangiocarcinoma, not TBX3’s role in the cancers named in the claim. Searches for TBX3 and for an oncogenic role in melanoma, breast, gastric, and cervical cancers found no passage addressing that point in our copy. (LLM, conf=0.76)
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Guo, T., Kouvonen, P., Koh, C. C., Gillet, L. C., Wolski, W. E., Röst, H. L., Rosenberger, G., Collins, B. C., Blum, L. C., Gillessen, S., et al. (2015) · Nature Medicine · doi:10.1038/nm.3807 · Cited by 376 · see citing works
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Cited by
Sorted by citations
Overexpression of TBX3 suppresses tumorigenesis in experimental and human cholangiocarcinoma
Deng, S., Lu, X., Wang, X., Liang, B., Xu, H., Yang, D., Cui, G., Yonemura, A., Paine, H., Zhou, Y., et al. (2024) · Cell Death & Disease · doi:10.1038/s41419-024-06839-8 · Cited by 2 · see citing works
- Authors
- Yi, X., Zhu, J., Liu, W., Peng, L., Lu, C., Sun, P., Huang, L., Nie, X., Huang, S., Guo, T., & Zhu, Y.
- Affiliations
- Westlake University (CN)
- Wuhan Union Hospital (CN)
- Zhejiang Library (CN)
- Huazhong University of Science and Technology (CN)
- Corresponding author
- Guo, Tiannan
- Zhu, Yi
- Venue
- Molecular & Cellular Proteomics
- Publisher
- Elsevier BV
- Published
- 2023-08
- Volume
- 22
- Issue
- 8
- Pages
- 100604
- ISSN
- 1535-9476 (ISSN-L)
- PMC
- PMC10413158
- OpenAlex
- W4381548205
- Cited by
- 25
- References
- 2
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 10
- FWCI
- 2.31
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecular & Cellular Proteomics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (21904107)
- National Key Research and Development Program of China (2021YFA1301602, 2022YF0608403)
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Health Sciences › Medicine › Hepatology › Hepatocellular Carcinoma Treatment and Prognosis
- Health Sciences › Medicine › Surgery › Cholangiocarcinoma and Gallbladder Cancer Studies
- Keywords
- hepatocellular carcinoma, intrahepatic cholangiocarcinoma, liver cancer, tumor proteome, lipid metabolism, extracellular matrix, cancer diagnosis
- MeSH terms
- Bile Duct Neoplasms, Bile Ducts, Intrahepatic, Carcinoma, Hepatocellular, Humans, Liver Neoplasms, Retrospective Studies, Cholangiocarcinoma, Proteome
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