Kato Taku, Mizutani Kosuke, Kawakami Kyojiro, Fujita Yasunori, Ehara Hidetoshi, Ito Masafumi
Department of Urology, Gifu University Graduate School of Medicine, Gifu 501-1193, Japan.
Department of Urology, Asahi University Hospital, Gifu 500-8523, Japan.
Heliyon. 2020 Jul 2;6(7):e04138. doi: 10.1016/j.heliyon.2020.e04138. eCollection 2020 Jul.
Docetaxel is first-line chemotherapy for castration-resistant prostate cancer (CRPC), but most patients acquire docetaxel resistance. CD44 has been shown to be involved in drug resistance of cancers including prostate cancer. We hypothesized that CD44 in serum exosomes could be a diagnostic marker for docetaxel resistance in CRPC patients. In this study, we examined CD44 protein and mRNA expression in cell lysates and exosomes isolated from prostate cancer cells, evaluated the effect of CD44v8-10 knockdown on docetaxel sensitivity and measured CD44 mRNA copy numbers contained in serum exosomes in prostate cancer patients.
Docetaxel-sensitive PC-3 prostate cancer cells and docetaxel-resistant PC-3R cells established previously from parental PC-3 cells were used. CD44v8-10 knockdown was performed by siRNA transfection. Blood was collected from 50 docetaxel-naïve and 10 docetaxel-resistant patients and 15 control males. CD44 protein expression was evaluated by Western blotting. CD44 mRNA expression was measured by RT-digital PCR.
The levels of CD44v8-10 protein and mRNA in cell lysates and exosomes were higher in PC-3R cells than in PC-3 cells. CD44v8-10 knockdown significantly increased docetaxel sensitivity of PC-3R cells. The CD44v8-10 mRNA copy numbers in serum exosomes were higher in docetaxel-resistant patients than in docetaxel-naïve patients and control males (median 46, 12 and 17 copies/mL serum, respectively, = 0.032). In contrast, the serum exosomal mRNA copy numbers of CD44 standard isoform (CD44s) were not different among 3 groups (median 25, 14 and 13 copies/mL serum, respectively, = 0.150).
CD44v8-10 may be involved in docetaxel resistance in prostate cancer and serum exosomal CD44v8-10 mRNA could be a diagnostic marker for docetaxel-resistant CRPC.
多西他赛是去势抵抗性前列腺癌(CRPC)的一线化疗药物,但大多数患者会产生多西他赛耐药性。已有研究表明,CD44参与包括前列腺癌在内的多种癌症的耐药过程。我们推测血清外泌体中的CD44可能是CRPC患者多西他赛耐药的诊断标志物。在本研究中,我们检测了前列腺癌细胞裂解物和外泌体中CD44蛋白和mRNA的表达,评估了CD44v8-10基因敲低对多西他赛敏感性的影响,并测定了前列腺癌患者血清外泌体中CD44 mRNA的拷贝数。
使用先前从亲代PC-3细胞建立的多西他赛敏感的PC-3前列腺癌细胞和多西他赛耐药的PC-3R细胞。通过siRNA转染进行CD44v8-10基因敲低。收集50例未接受多西他赛治疗的患者、10例多西他赛耐药患者和15例对照男性的血液。通过蛋白质印迹法评估CD44蛋白表达。通过RT-数字PCR测定CD44 mRNA表达。
PC-3R细胞裂解物和外泌体中CD44v8-10蛋白和mRNA水平高于PC-3细胞。CD44v8-10基因敲低显著提高了PC-3R细胞对多西他赛的敏感性。多西他赛耐药患者血清外泌体中CD44v8-10 mRNA拷贝数高于未接受多西他赛治疗的患者和对照男性(中位数分别为46、12和17拷贝/毫升血清,P = 0.032)。相比之下,3组中CD44标准异构体(CD44s)的血清外泌体mRNA拷贝数无差异(中位数分别为25、14和13拷贝/毫升血清,P = 0.150)。
CD44v8-10可能参与前列腺癌的多西他赛耐药,血清外泌体CD44v8-10 mRNA可能是多西他赛耐药CRPC的诊断标志物。