基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:STAT3 and PD-L1 are negatively correlated with ATM and have impact on the prognosis of triple-negative breast cancer patients with low ATM expression.
STAT3 and PD-L1 are negatively correlated with ATM and have impact on the prognosis of triple-negative breast cancer patients with low ATM expression.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
局部晚期 TNBC 且 ATM 低表达的患者可能更有可能从抗 PD-L1 抑制剂中获益。ATM 功能性抑制剂联合免疫检查点阻断疗法治疗 TNBC 的可行性也值得进一步探索。我们的研究表明,STAT3 在不同肿瘤中对肿瘤进展具有不同的影响。
三阴性乳腺癌(TNBC)以其侵袭性强、缺乏有效治疗而著称。程序性细胞死亡配体-1(PD-L1)抑制剂刚刚被批准用于晚期TNBC的治疗。为了准确筛选对抗PD-L1治疗敏感的TNBC,并探索共济失调毛细血管扩张突变蛋白(ATM)抑制剂联合PD-L1抑制剂、放疗和化疗的可行性,我们关注ATM是否通过c-Src、信号转导和转录激活因子1和3(STAT1和STAT3)参与PD-L1的调控并影响患者预后。
我们采用免疫组化染色,探讨86例病理III期TNBC中ATM与c-Src、STAT1、STAT3、PD-1/PD-L1、TIL(肿瘤浸润淋巴细胞)(TILs)以及其他临床病理特征的关系。同时还探讨了它们对预后的影响。
我们发现ATM表达与TNBC中的STAT1、STAT3、PD-L1、TILs和CD8+细胞呈负相关。STAT1与PD-L1的表达呈正相关。在ATM低表达的TNBC中,STAT3是预后改善的独立因素,而PD-L1是独立的负面预后因素。此外,在ATM低表达组中,c-Src第419位酪氨酸的磷酸化(p-c-src Y419)与STAT3的过表达相关。
We used immunohistochemical staining to explore the relationship of ATM with c-Src, STAT1, STAT3, PD-1/PD-L1, Tumor-infiltrating lymphocytes (TILs), as well as other clinicopathologic features in 86 pathological stage III TNBCs. Their impact on prognosis was also explored.
We found ATM expression was negatively correlated with STAT1, STAT3, PD-L1, TILs and CD8 + cells in TNBC. STAT1 positively correlated the expression of PD-L1. In TNBC with ATM low expression, STAT3 was an independent factor for improved prognosis, while PD-L1 was an independent negative prognostic factor. Furthermore, in low ATM group, the phosphorylation of tyrosine at position 419 of c-Src (p-c-src Y419) was correlated with the overexpression of STAT3.
Locally advanced TNBC with low ATM expression may be more likely to benefit from anti-PD-L1 inhibitors. The feasibility of ATM functional inhibitor combined with immune checkpoint blockade therapies in the treatment of TNBC is also worthy of further exploration. Our study suggests that STAT3 has different impacts on tumor progression in different tumors.
MEMBER ACCOUNT
登录成功会直接打开下一页。