Department of Pathology, Yeungnam University College of Medicine, Daegu, South Korea.
Department of Pathology, Yeungnam University Yeongcheon Hospital, Yeongcheon, South Korea.
Indian J Pathol Microbiol. 2022 Jul-Sep;65(3):598-603. doi: 10.4103/ijpm.ijpm_1256_21.
Cancer cells activate either telomerase or alternative lengthening of telomeres (ALT) to maintain telomere length and achieve immortalization. Alpha thalassemia/mental retardation X-linked (ATRX) is involved in chromatin remodeling. Mutations in ATRX genes are associated with the loss of nuclear expression and correlated with the ALT phenotype. ATRX expression has been evaluated in various cancers, especially sarcoma and neuroendocrine tumors, and its clinical significance has been shown to be diverse, depending on the tumor types. The role and prognostic value of ATRX expression in clear cell renal cell carcinoma (CCRCC) have not been elucidated.
We investigated the messenger RNA (mRNA) expression levels of ATRX using the gene expression profiling interactive analysis (GEPIA) database and evaluated the expression of ATRX using immunohistochemical (IHC) staining in 302 CCRCC cases.
Loss of ATRX expression was significantly associated with larger tumor size, higher nuclear grade (NG), lymphovascular invasion (LVI), pathologic T (pT) stage, recurrence/metastasis, and stage. Although ATRX was not an independent prognostic factor, patients with loss of ATRX expression showed poor survival.
Our findings suggest that loss of ATRX expression could be a potential biomarker for predicting aggressive tumor behavior and poor clinical outcomes in CCRCC.
癌细胞通过激活端粒酶或端粒的替代性延长(ALT)来维持端粒长度并实现永生化。α-地中海贫血/智力低下 X 连锁(ATRX)参与染色质重塑。ATRX 基因的突变与核表达的丧失有关,并与 ALT 表型相关。ATRX 表达已在各种癌症中进行了评估,特别是肉瘤和神经内分泌肿瘤,其临床意义因肿瘤类型而异。ATRX 表达在透明细胞肾细胞癌(CCRCC)中的作用和预后价值尚未阐明。
我们使用基因表达谱交互式分析(GEPIA)数据库研究了 ATRX 的信使 RNA(mRNA)表达水平,并使用免疫组织化学(IHC)染色在 302 例 CCRCC 病例中评估了 ATRX 的表达。
ATRX 表达缺失与肿瘤体积较大、核分级(NG)较高、脉管侵犯(LVI)、病理 T(pT)分期、复发/转移和分期有关。尽管 ATRX 不是独立的预后因素,但 ATRX 表达缺失的患者生存不良。
我们的研究结果表明,ATRX 表达缺失可能是预测 CCRCC 侵袭性肿瘤行为和不良临床结局的潜在生物标志物。