Department of Molecular Biology, São José do Rio Preto Medical School (FAMERP), São José do Rio Preto - SP, Brazil; Center for Research in Molecular Oncology, Barretos Cancer Hospital - Pio XII, Barretos - SP, Brazil.
Center for Research in Molecular Oncology, Barretos Cancer Hospital - Pio XII, Barretos - SP, Brazil.
Oral Oncol. 2014 Jun;50(6):587-92. doi: 10.1016/j.oraloncology.2014.02.015. Epub 2014 Mar 20.
Head and neck cancer is a collective term that describes malignant tumors of the oral cavity, pharynx, and larynx characterized by high incidence and mortality rates. Although most HNSCC originate from the mucosal surface of the upper aerodigestive tract, where they can be easily detected during a routine clinical examination. Often the definitive diagnosis is delayed because of the difficulty in differentiating from other similar lesions. Activation of proto-oncogenes and inactivation of tumor suppressor genes are the major molecular alterations involved in carcinogenesis. In addition, epigenetic changes can alter the expression of critical genes important in the development of a variety of cancers. The detection of aberrant gene promoter methylation as a tool for the detection of tumors or its use as prognostic marker have been described for many different cancers including HNSCC. The search for biomarkers has as its main aim the evaluation and measurement of the status of normal and pathological biological processes as well as pharmacological responses to certain treatments. The tracking of these biomarkers is an important part for the identification of individuals in the early stages of head and neck cancer for its diagnostic and prognostic relevance reflecting in high survival rates, better quality of life and less cost to the healthcare system. Therefore, assuming that cancer results from genetic and epigenetic changes, analyzes based on gene methylation profile in combination with the pathological diagnosis would be useful in predicting the behavior of these head and neck tumors.
头颈部癌症是一个总称,它描述了口腔、咽和喉的恶性肿瘤,其特点是发病率和死亡率高。虽然大多数 HNSCC 起源于上呼吸道的粘膜表面,在那里可以通过常规临床检查很容易地发现它们。然而,由于难以与其他类似病变区分开来,通常会延迟明确诊断。原癌基因的激活和肿瘤抑制基因的失活是致癌过程中主要的分子改变。此外,表观遗传变化可以改变在多种癌症发展中重要的关键基因的表达。异常基因启动子甲基化的检测作为肿瘤检测工具或作为预后标志物的用途已被描述用于许多不同的癌症,包括 HNSCC。寻找生物标志物的主要目的是评估和测量正常和病理生物过程的状态以及对某些治疗的药理反应。这些生物标志物的跟踪是识别头颈部癌症早期个体的重要部分,因为它反映了高生存率、更好的生活质量和对医疗保健系统的低费用,具有诊断和预后意义。因此,假设癌症是由遗传和表观遗传变化引起的,基于基因甲基化谱的分析结合病理诊断将有助于预测这些头颈部肿瘤的行为。