Fodor Dávid, Pozsgai Éva, Schally Andrew V, László Zoltán, Gömöri Éva, Szabó Éva, Rumi László, Lőcsei Dorottya, Boronkai Árpád, Bellyei Szabolcs
Department of Oncotherapy, Clinical Center, University of Pécs, Édesanyák Street 10, 7624 Pécs, Hungary.
Department of Public Health Medicine, Medical School, University of Pécs, Szigeti Street 12, 7624 Pécs, Hungary.
Biomedicines. 2023 Feb 27;11(3):719. doi: 10.3390/biomedicines11030719.
Rectal cancer constitutes nearly one-third of all colorectal cancer diagnoses, and certain clinical and molecular markers have been studied as potential prognosticators of patient survival. The main objective of our study was to investigate the relationship between the expression intensities of certain proteins, including growth-hormone-releasing hormone receptor (GHRH-R), Hsp90, Hsp16.2, p-Akt and SOUL, in specimens of locally advanced rectal cancer patients, as well as the time to metastasis and 10-year overall survival (OS) rates. We also investigated whether these outcome measures were associated with the presence of other clinical parameters.
In total, 109 patients were investigated retrospectively. Samples of pretreatment tumors were stained for the proteins GHRH-R, Hsp90, Hsp16.2, p-Akt and SOUL using immunhistochemistry methods. Kaplan-Meier curves were used to show the relationships between the intensity of expression of biomarkers, clinical parameters, the time to metastasis and the 10-year OS rate.
High levels of p-Akt, GHRH-R and Hsp90 were associated with a significantly decreased 10-year OS rate ( = 0.001, = 0.000, = 0.004, respectively) and high expression levels of p-Akt and GHRH-R were correlated with a significantly shorter time to metastasis. Tumors localized in the lower third of the rectum were linked to both a significantly longer time to metastasis and an improved 10-year OS rate.
Hsp 90, pAkt and GHRH-R as well as the lower-third localization of the tumor were predictive of the 10-year OS rate in locally advanced rectal cancer patients. The GHRH-R and Hsp90 expression levels were independent prognosticators of OS. Our results imply that GHRH-R could play a particularly important role both as a molecular biomarker and as a target for the anticancer treatment of advanced rectal cancer.
直肠癌占所有结直肠癌诊断病例的近三分之一,某些临床和分子标志物已被作为患者生存的潜在预后指标进行研究。我们研究的主要目的是调查局部晚期直肠癌患者标本中某些蛋白质的表达强度之间的关系,这些蛋白质包括生长激素释放激素受体(GHRH-R)、热休克蛋白90(Hsp90)、热休克蛋白16.2(Hsp16.2)、磷酸化蛋白激酶B(p-Akt)和SOUL,以及转移时间和10年总生存率(OS)。我们还研究了这些预后指标是否与其他临床参数的存在有关。
总共对109例患者进行了回顾性研究。使用免疫组织化学方法对预处理肿瘤样本进行GHRH-R、Hsp90、Hsp16.2、p-Akt和SOUL蛋白染色。采用Kaplan-Meier曲线来显示生物标志物表达强度、临床参数、转移时间和10年OS率之间的关系。
高水平的p-Akt、GHRH-R和Hsp90与显著降低的10年OS率相关(分别为P = 0.001、P = 0.000、P = 0.004),并且p-Akt和GHRH-R的高表达水平与显著缩短的转移时间相关。位于直肠下三分之一的肿瘤与显著更长的转移时间和改善的10年OS率相关。
Hsp90、pAkt和GHRH-R以及肿瘤的下三分之一定位可预测局部晚期直肠癌患者的10年OS率。GHRH-R和Hsp90表达水平是OS的独立预后指标。我们的结果表明,GHRH-R作为分子生物标志物和晚期直肠癌抗癌治疗靶点可能发挥特别重要的作用。