介质蛋白-31:炎症性细胞因子连接和癌症
Sabah Akhtar1, Fareed Ahmad1,2, Majid Alam1,2
1Translational Research Institute, Academic Health System, Hamad Medical Corporation, 3050 Doha, Qatar.
Frontiers in bioscience (Landmark edition)
|September 30, 2024
概括
介素31 (IL-31) 是一种促炎性细胞因子,与癌症和严重 () 有关. 本综述探讨了IL-31在癌症发展和症状严重性中的作用.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 皮肤病学 皮肤病学
背景情况:
- 干白素31 (IL-31) 是一种促炎性细胞因子,主要由II型辅助T细胞分泌.
- IL-31通过一个受体综合体发出信号,其中包括IL-31受体α和哥斯塔丁-M受体β.
- IL-31的关键病理作用是诱导 (),这是癌症患者常见和衰弱的症状.
研究的目的:
- 审查目前对IL-31在各种癌症类型的发病过程中的作用的理解.
- 阐明IL-31在瘤生物学中的确切参与,这在很大程度上仍然是难以捉摸的.
- 将IL-31在炎症性疾病中的已知功能与其对癌症的潜在影响联系起来.
主要方法:
- 文献综述和对IL-31现有研究的综合.
- 对研究不同类型瘤IL-31表达的研究进行分析.
- 检查IL-31,和癌症进展之间的关系.
主要成果:
- IL-31的表达因瘤类型而异,可能促进或抑制癌症的进展.
- 高IL-31表达与晚期瘤阶段和增加的严重程度有关.
- 和癌症的同时发生可能源于共同的蛋白质异常或间接的治疗效应.
结论:
- IL-31在癌症和之间的相互作用中发挥着重要作用.
- 需要进一步的研究才能充分理解IL-31在各种癌症病理中的复杂功能.
- 向IL-31可能为管理与癌症相关的症状和进展提供治疗潜力.
相关概念视频
T Cell Types and Functions
959
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
959
NF-κB-dependent Signaling Pathway
7.3K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
7.3K
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists
152
Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy. SP binds and activates...
152
Psychoneuroimmunology: Diabetes and Cancer
25
Chronic stress has been linked to both the onset and progression of serious health conditions, including Type 2 diabetes and cancer. Type 2 diabetes, a widespread chronic illness, is closely associated with obesity and insulin resistance, both of which often worsen under stress. Studies indicate that men experiencing high levels of chronic stress face a 45% higher risk of developing diabetes compared to those with minimal stress. Stress triggers physiological responses that elevate blood...
25
The Intrinsic Apoptotic Pathway
6.4K
Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
6.4K
The JAK-STAT Signaling Pathway
8.7K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
8.7K


