1. Molecular Stress and Stem Cell Biology Group, School of Biotechnology, KIIT University, Bhubaneswar, Odisha-751024, India.
2. Department of Surgical Oncology, Kalinga Institute of Medical sciences, Bhubaneswar, Odisha-751024, India. ; 5. Department of Surgical Oncology, Apollo Hospitals, Bhubaneswar, Odisha-751004, India.
J Cancer. 2015 Jan 15;6(2):192-202. doi: 10.7150/jca.9558. eCollection 2015.
Tumorigenesis is a complex process of accumulated alteration in function of multiple genes and pathways. Wnt signalling pathway is involved in various differentiation events during embryonic development and is conserved in various species.
A multicentre collaborative initiative is undertaken to study the occurrence, prognosis and molecular mechanism of HNSCC (Head and Neck Squamous Cell Carcinoma) which is highly prevalent in eastern parts of India. From a large cohort of HNSCC tissue repository, 67 cases were selected for multi-parametric investigation.
67 cases showed stable β-catenin expression. We have seen correlation, if any, of the transcription factor - β-catenin, telomere maintenance and shelterin complex proteins - TRF2, Rap1 and hTert with respect to tumor differentiation and telomere dysfunction. Immunohistochemistry of β-catenin protein showed stable and high expression in tumor when compared to stroma. MDSCC (Moderately Differentiated Squamous cell carcinoma) cases expressed nuclear expression of β-catenin in invasive fronts and showed increased genomic instability. Higher frequency of Anaphase bridges was observed ranging from <3% in normal cut margin to 13% in WDSCC (Well differentiated squamous cell carcinoma) and 18% in MDSCC (Moderately differentiated Squamous cell carcinoma). There was significant decrease in telomere length in MDSCC (<4) when compared to the normal cut margin samples (<7). Quantitative Real Time-PCR confirmed a significant correlationship between stable β-catenin expression and poor clinical and pathological outcome.
The Stabilisation and accumulation of β-catenin was significant and correlated well with de-differentiation process as well as prognosis and therapy outcome of the patients in the cohort. Expression status of molecular markers such as β-catenin, hTert, TRF2 and RAP1 correlate significantly with the process of tumorigenesis and prognosis and may play a role in therapeutic management of Head and neck patients.
肿瘤发生是一个复杂的过程,涉及多个基因和途径功能的累积改变。Wnt 信号通路参与胚胎发育过程中的各种分化事件,并在各种物种中保守。
一项多中心合作计划旨在研究在印度东部高发的头颈部鳞状细胞癌(HNSCC)的发生、预后和分子机制。从大量 HNSCC 组织库中,选择了 67 例进行多参数研究。
67 例病例β-连环蛋白表达稳定。我们观察到转录因子β-连环蛋白、端粒维持和庇护体复合物蛋白 TRF2、Rap1 和 hTert 是否与肿瘤分化和端粒功能障碍有关。β-连环蛋白蛋白的免疫组化显示,与基质相比,肿瘤中β-连环蛋白表达稳定且高。MDSCC(中分化鳞状细胞癌)病例在侵袭前沿表达核内β-连环蛋白,并表现出更高的基因组不稳定性。在正常切缘(<3%)和 WDSCC(高分化鳞状细胞癌)(13%)和 MDSCC(中分化鳞状细胞癌)(18%)中观察到的后期桥接频率显著增加。与正常切缘样本(<7)相比,MDSCC(<4)中端粒长度显著缩短。定量实时 PCR 证实稳定的β-连环蛋白表达与患者的临床和病理结局不良有显著相关性。
β-连环蛋白的稳定和积累与去分化过程以及队列中患者的预后和治疗结果显著相关。β-连环蛋白、hTert、TRF2 和 RAP1 等分子标志物的表达状态与肿瘤发生和预后显著相关,可能对头颈部患者的治疗管理发挥作用。