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Implications of anti-cytokine therapy in colorectal cancer and autoimmune diseases

机译:抗细胞因子治疗在大肠癌和自身免疫性疾病中的意义

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Up to 20% of all cancers have been linked to chronic inflammation and persistent infections. However, almost all solid tumours contain immune infiltrates, and tumour-associated inflammatory cells play broad roles in different stages of tumour development and malignant progression. Cytokines are important mediators of the inflammatory effect on tumorigenesis both in inflammation-induced cancer and in the inflammation that follows tumour development. We have shown interleukin (IL)-6 to be an important tumour promoter in early colitis-associated cancer (CAC). IL-6 is mainly produced by tumour-infiltrating myeloid cells under the control of NF-κB. IL-6 promotes proliferation of tumour-initiating cells derived from the intestinal epithelium and protects them from apoptotic elimination. These pro-survival and proliferative effects of IL-6 are mainly mediated by STAT3, whose ablation in intestinal epithelial cells significantly reduces CAC tumorigenesis. More recently, we found a critical role for IL-23 and its downstream cytokines IL-17 and IL-22 in the development of CAC. These findings suggest that such cytokines or the cells that produce them may provide new therapeutic or preventive targets in forms of colorectal cancer that are linked to inflammation.
机译:多达20%的癌症与慢性炎症和持续感染有关。然而,几乎所有实体瘤都含有免疫浸润物,并且与肿瘤相关的炎性细胞在肿瘤发展和恶性进展的不同阶段起着广泛的作用。细胞因子是炎症诱导的癌症和肿瘤发展后的炎症中对肿瘤发生的炎症作用的重要介质。我们已经显示白介素(IL)-6是早期结肠炎相关癌症(CAC)中的重要肿瘤启动子。 IL-6主要由肿瘤浸润的髓样细胞在NF-κB的控制下产生。 IL-6促进源自肠上皮的肿瘤引发细胞的增殖,并保护它们免受凋亡消除。 IL-6的这些促生存和增殖作用主要由STAT3介导,STAT3的消融作用可显着减少CAC的肿瘤发生。最近,我们发现IL-23及其下游细胞因子IL-17和IL-22在CAC的发展中起着关键作用。这些发现表明,这种细胞因子或产生它们的细胞可以以与炎症有关的结直肠癌形式提供新的治疗或预防靶标。

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