Senior Researcher, Laboratory of Molecular and Genetic Pathology, Department of Clinical Morphology; A. Tsyb Medical Radiological Research Centre - Branch of the National Medical Research Radiological Centre of the Ministry of Health of the Russian Federation, 4 Korolev St., Obninsk, 249036, Russia.
Head of the Laboratory for Quality Control of Medical Care; A. Tsyb Medical Radiological Research Centre - Branch of the National Medical Research Radiological Centre of the Ministry of Health of the Russian Federation, 4 Korolev St., Obninsk, 249036, Russia.
Sovrem Tekhnologii Med. 2021;13(3):33-38. doi: 10.17691/stm2021.13.3.04. Epub 2021 Jun 28.
was to identify and quantify lymphocytes with asynchronous replication of the and genes in cancer patients versus controls and to assess the diagnostic capabilities of this approach.
The study was carried out with peripheral blood lymphocytes probed for the and genes using the interphase fluorescence hybridization (FISH) method (Vysis, USA and Kreatech, The Netherlands). The control group included 70 people: clinically healthy donors and patients with non-oncological diseases such as gastritis, pancreatitis, chronic calculous cholecystitis, bronchial asthma, peptic ulcer disease, inguinal hernia, arthrosis, myoma, hepatitis, epilepsy, chronic prostatitis, chronic tonsillitis, and rectal adenoma. The group of cancer patients included 219 people with various oncological diseases: gastric cancer (n=68), colorectal cancer (n=30), chronic lymphocytic leukemia (n=52), Hodgkin lymphoma (n=33), and polyneoplasia (n=41).
In the control group, the mean frequency of lymphocytes with asynchronous gene replication (AGR) was 22.0±3.4% for and 18.0±3.2% for ; in the group of cancer patients, that was 36.8±4.8 and 28.4±5.1%, respectively. The excessive presence of lymphocytes with the AGR in cancer patients was consistent and statistically significant (p<0.0001). For the gene, the AGR-based cancer detection showed a sensitivity of 98.6±0.7%, a specificity of 100%, and an accuracy of 98.3±0.8%, and for the gene - 78.6±3.1, 98.5±0.9, and 85.9±2.6%, respectively.
This pilot study on lymphocytes with AGR of and genes in cancer patients can serve a basis for creating a new molecular cytogenetic technology for detecting malignant neoplasms in humans.
鉴定和量化癌症患者与对照个体外周血淋巴细胞中 和 基因复制的异时性,并评估该方法的诊断能力。
本研究采用间期荧光原位杂交(FISH)法(美国 Vysis 和荷兰 Kreatech),对 和 基因进行外周血淋巴细胞探测。对照组包括 70 人:临床健康供者及非肿瘤性疾病患者,如胃炎、胰腺炎、慢性结石性胆囊炎、支气管哮喘、消化性溃疡病、腹股沟疝、关节炎、子宫肌瘤、肝炎、癫痫、慢性前列腺炎、慢性扁桃体炎和直肠腺瘤。癌症患者组包括 219 名患有各种肿瘤性疾病的患者:胃癌(n=68)、结直肠癌(n=30)、慢性淋巴细胞白血病(n=52)、霍奇金淋巴瘤(n=33)和多发性肿瘤(n=41)。
在对照组中, 和 基因复制异时性(AGR)的淋巴细胞平均频率分别为 22.0±3.4%和 18.0±3.2%;在癌症患者组中,该值分别为 36.8±4.8%和 28.4±5.1%。癌症患者中存在大量具有 AGR 的淋巴细胞,这一现象具有一致性且具有统计学意义(p<0.0001)。对于 基因,基于 AGR 的癌症检测具有 98.6±0.7%的灵敏度、100%的特异性和 98.3±0.8%的准确性,而对于 基因则分别为 78.6±3.1%、98.5±0.9%和 85.9±2.6%。
本研究初步探讨了癌症患者中 和 基因复制异时性的淋巴细胞,可为创建一种新的人类恶性肿瘤分子细胞遗传学检测技术奠定基础。