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Open AccessJournal ArticleDOI

Hepatocellular Carcinoma: Etiology and Current and Future Drugs.

Aastha Jindal, +2 more
- 01 Mar 2019 - 
- Vol. 9, Iss: 2, pp 221-232
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TLDR
There is an urgent need for new systemic combination therapies that target different signaling mechanisms, thereby decreasing the prospect of cancer cells developing resistance to treatment, and currently approved drugs and other potential candidates of HCC such as Milcic lib, palbociclib, galunisertib, ipafricept, and ramucirumab are evaluated.
Abstract
Hepatocellular carcinoma (HCC) is swiftly increasing in prevalence globally with a high mortality rate. The progression of HCC in patients is induced with advanced fibrosis, mainly cirrhosis, and hepatitis. The absence of proper preventive or curative treatment methods encouraged extensive research against HCC to develop new therapeutic strategies. The Food and Drug Administration-approved Nexavar (sorafenib) is used in the treatment of patients with unresectable HCC. In 2017, Stivarga (regorafenib) and Opdivo (nivolumab) got approved for patients with HCC after being treated with sorafenib, and in 2018, Lenvima (lenvatinib) got approved for patients with unresectable HCC. But, owing to the rapid drug resistance development and toxicities, these treatment options are not completely satisfactory. Therefore, there is an urgent need for new systemic combination therapies that target different signaling mechanisms, thereby decreasing the prospect of cancer cells developing resistance to treatment. In this review, HCC etiology and new therapeutic strategies that include currently approved drugs and other potential candidates of HCC such as Milciclib, palbociclib, galunisertib, ipafricept, and ramucirumab are evaluated.

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Immunotherapy for hepatocellular carcinoma.

TL;DR: An overview of the liver immunoanatomy, the potential immune mechanisms of HCC, and current (pre)clinical developments in this field is provided.
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Circ_0001955 facilitates hepatocellular carcinoma (HCC) tumorigenesis by sponging miR-516a-5p to release TRAF6 and MAPK11

TL;DR: It is revealed that circ_0001955, TRAF6 and MAPK11 levels were increased, while miR-516a-5p levels were decreased in HCC tumor tissues compared to adjacent normal tissues.
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Multikinase Inhibitor Treatment in Thyroid Cancer.

TL;DR: The novel therapeutic regimen with MKIs has shown favorable results in otherwise treatment-resistant thyroid cancer, and it is important to focus on the management of AEs for a decent long-term outcome.
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MAPK/ERK Signaling Pathway in Hepatocellular Carcinoma

TL;DR: The MAPK/ERK signaling pathway is activated in more than 50% of human HCC cases; however, activating mutations in RAS and RAF genes are rarely found in HCC as mentioned in this paper.
Journal ArticleDOI

Etiology of Hepatocellular Carcinoma: Special Focus on Fatty Liver Disease.

TL;DR: The etiology of HCC is recapitulates, focusing especially on the nonalcoholic fatty liver disease (NAFLD)- and alcoholic fatty Liver disease (AFLD-associated HCC), with a focus on chronic liver inflammation and injury.
References
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Journal ArticleDOI

Epidemiology of Viral Hepatitis and Hepatocellular Carcinoma

TL;DR: This review summarizes the risk factors for HCC among HBV- or HCV-infected individuals, based on findings from epidemiologic studies and meta-analyses, as well as determinants of patient outcome and the HCC disease burden, globally and in the United States.
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