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:PFKP: A biomarker for prognosis, response to treatment and immune function of breast cancer.
PFKP: A biomarker for prognosis, response to treatment and immune function of breast cancer.
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。
背景磷酸果糖激酶-血小板型(PFKP)是糖酵解中的限速酶。PFKP在包括乳腺癌在内的多种癌症类型中高表达。目的评估PFKP作为乳腺癌预后指标的程度及其预测治疗反应的能力。
进一步理解PFKP与癌症进展中关键信号通路、免疫系统及表观遗传学之间的相互作用。方法利用在线平台(Kaplan-Meier绘图仪、受试者工作特征曲线绘图仪、cBioPortal和肿瘤-免疫系统相互作用数据库(TISIDB)),进行生物信息学分析,以确定与乳腺癌中PFKP表达相关的预后和预测效应。使用Oncomine平台进行网络分析,研究信号、表观遗传和免疫调节通路。结果PFKP在乳腺癌中具有不良预后效应,在RNA和蛋白质水平上均得到证实。这种效应在晚期乳腺癌中尤为显著。PFKP似乎在进展生命周期早期即招募标志性癌症通路,从导管原位癌到晚期癌症。PFKP是luminal A型乳腺癌和三阴性乳腺癌短期化疗耐药的生物标志物,也是luminal B型乳腺癌长期内分泌治疗敏感性的生物标志物。PFKP与免疫系统组分如TIL(肿瘤浸润淋巴细胞)、趋化因子和免疫调节剂相互作用。结论PFKP在乳腺癌中过表达并具有不良预后效应,尤其是在侵袭性亚型和晚期疾病中。它在标志性癌症通路中发挥关键作用,并与免疫系统相互作用,这些相互作用方式可为未来的治疗开发所利用。
BackgroundPhosphofructokinase-platelet (PFKP) is a rate-limiting enzyme in glycolysis. PFKP is highly expressed across many cancer types including breast cancer. PurposeTo assess the extent to which PFKP can be a prognostic indicator in breast cancer and its ability to predict treatment response. To further understanding of the interaction between PFKP and key signaling pathways in cancer progression, the immune system, and epigenetics. MethodsUsing online platforms (Kaplan-Meier plotter, receiver operating characteristic curve plotter, cBioPortal, and Tumor-Immune System Interaction Database (TISIDB)), a bioinformatic analysis was conducted to establish the prognostic and predictive effects related to PFKP expression in breast cancer. A network analysis was performed using the Oncomine platform where signaling, epigenetic, and immune regulation pathways were investigated.
ResultsPFKP had a poor prognostic effect in breast cancer, demonstrated at both the RNA and protein levels. This effect was prominent in advanced breast cancers. PFKP appeared to recruit hallmark cancer pathways early in the progression lifecycle, from ductal carcinoma in situ to advanced cancer. PFKP was a biomarker of resistance to chemotherapy in the short-term for luminal A breast cancer and triple-negative breast cancer, and of sensitivity to endocrine therapy over the long term for luminal B breast cancer.
PFKP interacts with immune system components such tumor-infiltrating lymphocytes, chemokines, and immunomodulators. ConclusionsPFKP is overexpressed in breast cancer and has a poor prognostic effect, particularly in aggressive subtypes and advanced disease. It plays a key role in hallmark cancer pathways and interacts with the immune system in ways that could be harnessed for future therapeutic development.
MEMBER ACCOUNT
登录成功会直接打开下一页。