Lobinger Dominik, Taylor Nicholas, Messner Verena, Seier Sophie, Bodner Johannes, Roberts Erika, Dezfouli Ali Bashiri, Pockley Alan Graham, Safi Seyer, Multhoff Gabriele
Department of Thoracic Surgery, München Klinik Bogenhausen, Lehrkrankenhaus der Technischen Universität München (TUM), 81925, Munich, Germany.
Central Institute for Translational Cancer Research Technische Universität München (TranslaTUM), TUM School of Medicine and Health, Klinikum rechts der Isar, Technische Universität München (TUM), 81675, Munich, Germany.
BMC Cancer. 2025 Aug 9;25(1):1297. doi: 10.1186/s12885-025-14725-5.
Heat shock protein 70 (Hsp70) which is frequently overexpressed in many different cancer types is also present on the plasma membrane of tumor but not normal cells. The intensity of membrane-expressed Hsp70 (mHsp70) is associated with disease progression and treatment resistance. It has also been shown that Hsp70 can be actively released into the circulation by mHsp70 positive, viable tumor cells in the form of extracellular lipid microvesicles expressing mHsp70, the levels of which might therefore act as a potential biomarker for tumor aggressiveness in lung malignancies.
Extracellular Hsp70 (eHsp70) was measured in the plasma of patients with non-small cell lung cancer (n = 178, NSCLC) and lung metastases of extrathoracic tumors (n = 35) prior to surgery using the Hsp70-exo ELISA which detects microvesicle-associated eHsp70 and the patient`s immunophenotype was determined by flow cytometric analysis of the corresponding peripheral blood lymphocytes.
eHsp70 values were significantly higher in patients with NSCLC than in healthy individuals, with no differences between adeno and squamous cell carcinomas. Levels of circulating eHsp70 which are associated with the Programmed cell death protein 1 (PD-L1) status, gradually increased from early stage to metastatic disease, and patients with lymph node metastases in surgically treatable NSCLC had significantly higher eHsp70 levels than nodal negative patients. In all tumor stages, total lymphocyte counts were significantly reduced and immunoregulatory T (Treg) cell counts were increased compared to healthy controls. Lower CD4 + T helper cell and higher CD3-/CD56+/CD94+/CD69+/NKp30+/NKp46 + NK cell ratios were only found in patients with thoracic metastases of other primary tumors. An early relapse after complete resection with curative intent correlated with significantly elevated eHsp70 levels which were measured prior to surgery, in all thoracic cancer patients.
In summary, we propose circulating eHsp70 levels before any treatment as a predictive biomarker for the presence of lymph node metastases and early therapy failure in patients with thoracic malignancies.
热休克蛋白70(Hsp70)在许多不同类型的癌症中经常过度表达,也存在于肿瘤细胞而非正常细胞的质膜上。膜表达热休克蛋白70(mHsp70)的强度与疾病进展和治疗耐药性相关。研究还表明,Hsp70可以由mHsp70阳性的存活肿瘤细胞以表达mHsp70的细胞外脂质微泡的形式主动释放到循环中,因此其水平可能作为肺恶性肿瘤中肿瘤侵袭性的潜在生物标志物。
在手术前,使用检测微泡相关细胞外Hsp70(eHsp70)的Hsp70-exo ELISA法,检测非小细胞肺癌患者(n = 178,NSCLC)和胸外肿瘤肺转移患者(n = 35)血浆中的eHsp70,并通过对相应外周血淋巴细胞的流式细胞术分析确定患者的免疫表型。
NSCLC患者的eHsp70值显著高于健康个体,腺癌和鳞癌之间无差异。与程序性细胞死亡蛋白1(PD-L1)状态相关的循环eHsp70水平从早期到转移性疾病逐渐升高,可手术治疗的NSCLC患者中伴有淋巴结转移的患者eHsp70水平显著高于无淋巴结转移的患者。在所有肿瘤阶段,与健康对照相比,总淋巴细胞计数显著减少,免疫调节性T(Treg)细胞计数增加。仅在其他原发性肿瘤胸内转移患者中发现较低的CD4 + T辅助细胞和较高的CD3-/CD56+/CD94+/CD69+/NKp30+/NKp46 + NK细胞比率。在所有胸段癌症患者中,根治性切除术后早期复发与术前测量的显著升高的eHsp70水平相关。
总之,我们建议将任何治疗前的循环eHsp70水平作为胸段恶性肿瘤患者存在淋巴结转移和早期治疗失败的预测生物标志物。