The roles of Hedgehog signalling and NF-κB activity in pancreatic cancer and opportunities for treatment

Q2 Agricultural and Biological Sciences Bioscience Horizons Pub Date : 2014-06-01 DOI:10.1093/BIOHORIZONS/HZU004
J. Ranson
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引用次数: 4

Abstract

Pancreatic cancer is the seventh most common form of cancer-related death in the world, affecting hundreds of thousands of people worldwide every year. Treatment for this type of cancer is largely ineffective and future treatments are likely to involve targeting signalling pathways involved in the proliferation of pluripotent stem cells. There are a variety of signalling pathways involved in the pathogenesis of the disease, including Hedgehog (Hh) and nuclear factor-kappaB (NF- κ B). Overexpression of Hh ligands or alterations in other areas of the Hh signalling pathway may lead to tumour formation. Inhibition of Hh ligands, Smoothened or Gli proteins, or up-regulation of Patched expression, could form the basis of new treatments. NF- κ B is often active in pancreatic cancer cells and down-regulation of NF- κ B activating molecules can inhibit tumour progression in cell culture studies. Clinical trials show some promising results in novel drugs. There is growing evidence to suggest the interaction between these two signalling pathways. NF- κ B appears to play a role upstream of the Hh pathway. This article looks at the roles these pathways play in pancreatic cancer and explores current research into targeting them for treatment.
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Hedgehog信号和NF-κB活性在胰腺癌中的作用及治疗机会
胰腺癌是世界上第七大最常见的癌症相关死亡形式,每年影响全球数十万人。这类癌症的治疗在很大程度上是无效的,未来的治疗可能涉及靶向与多能干细胞增殖有关的信号通路。该疾病的发病机制涉及多种信号通路,包括Hedgehog (Hh)和核因子κ B (NF- κ B), Hh配体的过表达或Hh信号通路其他区域的改变可能导致肿瘤的形成。抑制Hh配体、Smoothened或Gli蛋白,或上调Patched蛋白的表达,可能成为新疗法的基础。在细胞培养研究中,NF- κ B在胰腺癌细胞中经常活跃,下调NF- κ B激活分子可以抑制肿瘤进展。新药的临床试验显示出一些有希望的结果。越来越多的证据表明,这两种信号通路之间存在相互作用。NF- κ B似乎在Hh通路的上游发挥作用。本文着眼于这些通路在胰腺癌中的作用,并探讨了目前针对它们进行治疗的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioscience Horizons
Bioscience Horizons Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
1.50
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0.00%
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0
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