Metabolic networks in mutant KRAS-driven tumours: tissue specificities and the microenvironment.

Metabolic networks in mutant KRAS-driven tumours: tissue specificities and the microenvironment.
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DOI:
10.1038/s41568-021-00375-9
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发表时间:
2021-08
期刊:
Nature reviews. Cancer
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其他
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KRAS中的致癌突变驱动常见的代谢程序,促进结直肠癌,非小细胞肺癌和胰腺导管腺癌的肿瘤生存,生长和免疫逃避。然而,突变KRAS信号传导对恶性细胞程序和肿瘤性质的影响也取决于肿瘤抑制因子的丧失和对细胞和组织起源特异的生理特征。在这里,我们审查收敛和不同的代谢网络调节致癌突变KRAS在结肠,肺和胰腺肿瘤,重点是共同发生的突变和肿瘤微环境的作用。此外,我们探讨了如何利用这些网络获得治疗效果。
Oncogenic mutations in KRAS drive common metabolic programmes that facilitate tumour survival, growth and immune evasion in colorectal carcinoma, non-small-cell lung cancer and pancreatic ductal adenocarcinoma. However, the impacts of mutant KRAS signalling on malignant cell programmes and tumour properties are also dictated by tumour suppressor losses and physiological features specific to the cell and tissue of origin. Here we review convergent and disparate metabolic networks regulated by oncogenic mutant KRAS in colon, lung and pancreas tumours, with an emphasis on co-occurring mutations and the role of the tumour microenvironment. Furthermore, we explore how these networks can be exploited for therapeutic gain.
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