Immunomodulatory TGF-β Signaling in Hepatocellular Carcinoma. Issue 11 (November 2019)
- Record Type:
- Journal Article
- Title:
- Immunomodulatory TGF-β Signaling in Hepatocellular Carcinoma. Issue 11 (November 2019)
- Main Title:
- Immunomodulatory TGF-β Signaling in Hepatocellular Carcinoma
- Authors:
- Chen, Jian
Gingold, Julian A.
Su, Xiaoping - Abstract:
- Abstract : Hepatocellular carcinoma (HCC) is an inflammation-induced and chemotherapy-resistant cancer. Dysregulated signaling in the transforming growth factor beta (TGF-β) pathway plays a central role in inflammation, fibrogenesis, and immunomodulation in the HCC microenvironment. This review dissects the genetic landscape of the TGF-β superfamily genes in HCC and discusses the essential effects of this pathway on the tumor immune microenvironment. We highlight the TGF-β signature as a potential biomarker for identifying individualized immunotherapeutic approaches in HCC. An improved understanding of the detailed mechanisms of liver cancer immunogenicity and the specific role of TGF-β in mediating immunotherapy resistance in HCC will provide important insights into HCC immune escape and promote the development of biomarker-derived combination immunotherapies for HCC. Highlights: Highly activated TGF-β in hepatocellular carcinoma (HCC) is significantly associated with immune cell exhaustion, while inactivated TGF-β is correlated with impaired DNA repair. The combination of TGF-β inhibitors and immune-checkpoint inhibitors successfully induced complete responses in mouse cancer models, highlighting the key immunosuppressive role of TGF-β signaling in regulating HCC immunotherapy. A novel immune-based classification identified three HCC tumor classes in the tumor microenvironment: the immune class, the intermediate immune class, and the immune exclusion class. Treatment ofAbstract : Hepatocellular carcinoma (HCC) is an inflammation-induced and chemotherapy-resistant cancer. Dysregulated signaling in the transforming growth factor beta (TGF-β) pathway plays a central role in inflammation, fibrogenesis, and immunomodulation in the HCC microenvironment. This review dissects the genetic landscape of the TGF-β superfamily genes in HCC and discusses the essential effects of this pathway on the tumor immune microenvironment. We highlight the TGF-β signature as a potential biomarker for identifying individualized immunotherapeutic approaches in HCC. An improved understanding of the detailed mechanisms of liver cancer immunogenicity and the specific role of TGF-β in mediating immunotherapy resistance in HCC will provide important insights into HCC immune escape and promote the development of biomarker-derived combination immunotherapies for HCC. Highlights: Highly activated TGF-β in hepatocellular carcinoma (HCC) is significantly associated with immune cell exhaustion, while inactivated TGF-β is correlated with impaired DNA repair. The combination of TGF-β inhibitors and immune-checkpoint inhibitors successfully induced complete responses in mouse cancer models, highlighting the key immunosuppressive role of TGF-β signaling in regulating HCC immunotherapy. A novel immune-based classification identified three HCC tumor classes in the tumor microenvironment: the immune class, the intermediate immune class, and the immune exclusion class. Treatment of tumors in each class is likely to require specific immunotherapeutic approaches. Deep single-cell RNA sequencing of tumor-infiltrating lymphocytes identified molecular characteristics in the microenvironment that may guide future therapeutic strategies. … (more)
- Is Part Of:
- Trends in molecular medicine. Volume 25:Issue 11(2019)
- Journal:
- Trends in molecular medicine
- Issue:
- Volume 25:Issue 11(2019)
- Issue Display:
- Volume 25, Issue 11 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 11
- Issue Sort Value:
- 2019-0025-0011-0000
- Page Start:
- 1010
- Page End:
- 1023
- Publication Date:
- 2019-11
- Subjects:
- hepatocellular carcinoma -- TGF-β signaling -- immune genomic profiling -- tumor microenvironment -- immunotherapy
Molecular biology -- Periodicals
Pathology, Molecular -- Periodicals
Physiology, Pathological -- Periodicals
572.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14714914 ↗
http://www.elsevier.com/locate/issn/14714914 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/14714914 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/14714914 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molmed.2019.06.007 ↗
- Languages:
- English
- ISSNs:
- 1471-4914
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9049.666000
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- 12066.xml