Eckel-Passow Jeanette E, Serie Daniel J, Cheville John C, Ho Thai H, Kapur Payal, Brugarolas James, Thompson R Houston, Leibovich Bradley C, Kwon Eugene D, Joseph Richard W, Parker Alexander S
Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
Department of Health Sciences Research, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
BMC Urol. 2017 Mar 21;17(1):19. doi: 10.1186/s12894-017-0209-3.
BAP1 and PBRM1 are frequently mutated in primary clear cell renal cell carcinoma (ccRCC) tumors; however, the frequency and clinical relevance of these mutations in metastatic ccRCC tumors is unknown. Additionally, while intra-tumor heterogeneity has been shown to be common in primary ccRCC, little is known regarding heterogeneity in metastatic ccRCC tumors.
We analyzed BAP1 and PBRM1 loss of protein expression in patient-matched primary and metastatic tumors from 97 patients. Expression was determined using a validated immunohistochemistry assay, which has been shown to be correlated with mutation status.
Of the 97 patients evaluated, 20 and 57% showed loss of BAP1 and PBRM1 in their primary tumors, respectively. Comparing expression across patient-matched primary-metastatic tumor pairs, 98 and 90% had concordant BAP1 and PBRM1 expression, respectively. Both patients who demonstrated discordant BAP1 expression showed loss of BAP1 expression during progression to metastatic ccRCC. Similarly, seven of the ten patients that demonstrated discordant PBRM1 expression showed loss of PBRM1 expression during progression to metastatic ccRCC. We evaluated intra-metastatic tumor heterogeneity using 12 patients who had multiple blocks available from the same tumor with representative pathology; 100 and 92% showed concordant BAP1 and PBRM1 expression, respectively. Amongst 32 patients who had serial metastatic tumors available, both BAP1 and PBRM1 had 97% concordant expression.
We observed minimal intra- and inter- tumor heterogeneity in metastatic ccRCC tumors. Patients with discordant BAP1 or PBRM1 expression across their matched primary and metastatic tumors usually showed loss of expression during progression to metastatic ccRCC.
BAP1和PBRM1在原发性透明细胞肾细胞癌(ccRCC)肿瘤中经常发生突变;然而,这些突变在转移性ccRCC肿瘤中的频率和临床相关性尚不清楚。此外,虽然肿瘤内异质性在原发性ccRCC中很常见,但对于转移性ccRCC肿瘤中的异质性知之甚少。
我们分析了97例患者配对的原发性和转移性肿瘤中BAP1和PBRM1蛋白表达缺失情况。使用经过验证的免疫组织化学检测方法确定表达情况,该方法已被证明与突变状态相关。
在评估的97例患者中,分别有20%和57%的患者原发性肿瘤中出现BAP1和PBRM1表达缺失。比较配对的原发性-转移性肿瘤对之间的表达情况,分别有98%和90%的患者BAP1和PBRM1表达一致。在原发性和转移性肿瘤中BAP1表达不一致的两名患者在进展为转移性ccRCC过程中均出现BAP1表达缺失。同样,在原发性和转移性肿瘤中PBRM1表达不一致的10例患者中有7例在进展为转移性ccRCC过程中出现PBRM1表达缺失。我们使用12例同一肿瘤有多个具有代表性病理切片的患者评估肿瘤内转移异质性;分别有100%和92%的患者BAP1和PBRM1表达一致。在有连续转移性肿瘤的32例患者中,BAP1和PBRM1的表达一致性均为97%。
我们观察到转移性ccRCC肿瘤中肿瘤内和肿瘤间异质性极小。在配对的原发性和转移性肿瘤中BAP1或PBRM1表达不一致的患者在进展为转移性ccRCC过程中通常出现表达缺失。