在癌症进展过程中,BST2诱导了血管光滑肌肉细胞可塑性和表型切换
bioRxiv : the preprint server for biology
|September 24, 2024
概括
顺肌细胞 (SMCs) 可以在瘤中采用类似巨细胞的表型,潜在地影响瘤微环境. 这种由BST2信号驱动的可塑性可能会导致免疫抑制,并影响癌症治疗结果.
科学领域:
- 细胞生物学 细胞生物学
- 癌症生物学 癌症生物学
- 免疫学 免疫学 免疫学
背景情况:
- 顺肌细胞 (SMC) 的可塑性与各种疾病有关,但其在瘤发生中的作用尚不清楚.
- 研究瘤血管生成和瘤微环境中的SMC多样性和可塑性至关重要.
研究的目的:
- 确定SMC多样性和可塑性是否以及如何影响瘤血管生成和瘤微环境.
- 在癌症的背景下阐明驱动SMC表型切换的机制.
主要方法:
- 利用了SMC特定的谱系追踪小鼠模型和单细胞RNA测序.
- 采用CellChat联体受体算法进行信号通路的计算预测.
- 进行了体外SMC测定以验证表型变化和功能改变.
主要成果:
- 瘤中显著比例的SMC采用了类似巨的表型,类似于M2b巨.
- 从瘤细胞向SMC传递BST2信号 (通过PIRA2) 促进了这种过渡,增强了SMC的增殖,迁移和细胞能力.
- BST2倒置减少了SMC表型切换,切换细胞表现出与抗瘤效应相关的炎症信号增加.
结论:
- 现型交换的SMC可能会导致免疫抑制性瘤微环境 (TME),因为BST2是与M2巨细胞倾斜相关的不良预后标志物.
- 这些发现表明,SMC可塑性在癌症病原和免疫逃避中起着新的作用.
- 需要进一步的研究来探索在癌症治疗中准SMC可塑性的治疗潜力.
更多相关视频
08:28Isolation of Primary Patient-specific Aortic Smooth Muscle Cells and Semiquantitative Real-time Contraction Measurements In Vitro
Published on: February 15, 2022
3.6K
06:54Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
12.8K
相关概念视频
Adaptive Mechanisms in Cancer Cells
5.7K
Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
5.7K
Metastasis
5.5K
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
5.5K
Cancer Stem Cells and Tumor Maintenance
4.9K
Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
4.9K
Tumor Progression
6.3K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
6.3K
TGF - β Signaling Pathway
7.3K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.3K
mTOR Signaling and Cancer Progression
3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.8K
