Division of Cancer Medicine and Blood Diseases, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California 90033, USA.
Clin Cancer Res. 2010 Sep 15;16(18):4675-80. doi: 10.1158/1078-0432.CCR-10-1113. Epub 2010 Jul 29.
In addition to their expression on pituitary cells, receptors for luteinizing hormone-releasing hormone (LH-RH) are found on most prostate cancer cells. These tumoral LH-RH receptors mediate the direct cytotoxic effects of LH-RH analogs and are potential therapeutic targets. Although pituitary LH-RH receptors are downregulated following prolonged exposure to LH-RH agonists, there is no evidence that tumoral receptors behave in a similar manner. To better characterize expression of tumoral LH-RH receptors, specimens of prostate cancer from various cohorts of patients were analyzed.
Surgical specimens were obtained from untreated patients with prostate cancer and from patients with metastatic castration-resistant prostate cancer previously treated with bilateral orchiectomy. To address the possibility of receptor downregulation, two additional cohorts of patients who had been previously treated with LH-RH agonists were included. One group received neoadjuvant therapy prior to prostatectomy, and the other group was treated for metastatic disease with LH-RH agonists and, at progression, required palliative resection of the prostate. Lymph node metastases from previously untreated patients were subjected to similar analysis.
Expression of LH-RH receptors was found in most specimens. The relative expression of LH-RH receptor mRNA in untreated patients was greater in patients whose tumor had received a Gleason score <8.
LH-RH receptor expression persisted despite prolonged exposure to LH-RH agonists. These findings support the concept of targeting cytotoxic LH-RH analogs to prostatic LH-RH receptors, using these receptors to gain entry into cancer cells to deliver a hybridized cytotoxic moiety for the treatment of prostate cancer.
除了在垂体细胞上表达外,黄体生成素释放激素 (LH-RH) 的受体也存在于大多数前列腺癌细胞上。这些肿瘤 LH-RH 受体介导 LH-RH 类似物的直接细胞毒性作用,是潜在的治疗靶点。虽然垂体 LH-RH 受体在长期暴露于 LH-RH 激动剂后会下调,但没有证据表明肿瘤受体会以类似的方式发挥作用。为了更好地描述肿瘤 LH-RH 受体的表达情况,分析了来自不同患者队列的前列腺癌标本。
从未经治疗的前列腺癌患者和先前接受双侧睾丸切除术治疗转移性去势抵抗性前列腺癌的患者获得手术标本。为了解决受体下调的可能性,还包括了另外两组先前接受 LH-RH 激动剂治疗的患者。一组患者在前列腺切除术前接受新辅助治疗,另一组患者接受 LH-RH 激动剂治疗转移性疾病,在进展时需要进行前列腺姑息性切除术。对未接受治疗的患者的淋巴结转移进行了类似的分析。
在大多数标本中发现了 LH-RH 受体的表达。在未接受治疗的患者中,肿瘤 Gleason 评分<8 的患者的 LH-RH 受体 mRNA 相对表达更高。
尽管长期暴露于 LH-RH 激动剂,但 LH-RH 受体的表达仍然存在。这些发现支持使用这些受体将细胞毒性 LH-RH 类似物靶向前列腺 LH-RH 受体的概念,利用这些受体进入癌细胞,输送杂交细胞毒性部分用于治疗前列腺癌。