Yang Tingting, Gu Jingjing, Liu Ting, Ma Haibin, Ma Xiaona, Tao Jin, Jin Yiran, Liang Xueyun
Institute of Human Stem Cell Research, General Hospital of Ningxia Medical University, Yinchuan 750004, China.
College of Clinical Medicine, General Hospital of Ningxia Medical University, Yinchuan 750004, China.
Zhongguo Fei Ai Za Zhi. 2018 Jun 20;21(6):431-436. doi: 10.3779/j.issn.1009-3419.2018.06.01.
Tumor recurrence and drug resistance are the main causes of death in tumor patients. The family of acetaldehyde dehydrogenase (ALDH) is closely related to the proliferation, migration, invasion and resistance of tumor cells, and different ALDH subtypes are expressed in different tumor cells. The aim of this study is to elucidate the ALDH subtype in human lung adenocarcinoma HCC-827/GR cells, which resistant to the gefitinib.
The human lung adenocarcinoma HCC-827 cells were used to generate the gefitinib-resistant HCC-827/GR cells; the expression of ALDH subtype in either HCC-827 or HCC-827/GR was detected by flow cytometry; The proliferative capacity and sensitivity to gefitinib of hcc-827/GR cells were analyzed by MTT assay before and after treatment with 100 μmol/L diethyllaminaldehyde (DEAB); Real-time quantitative PCR was used to detect the expression of ALDH subtypes at mRNA levels in hcc-827 cells and hcc-827/GR cells.
Compared with HCC-827 cells, the positive rate of ALDH in HCC-827/GR cells increased. The proliferation ability of HCC-827/GR cells decreased after treatment with 100 μmol/L DEAB. Compared with HCC-827 cells, the expression of ALDH1A1 and ALDH1L1 mRNA was increased in hcc-827/GR cells, but the ALDH3B2 expression was decreased.
ALDH might be used as a molecular biomarker to test the gefitinib-resistant to lung adenocarcinoma cancer cells, and the ALDH1A1 may play a role in gefitinib resistance in lung cancer.
肿瘤复发和耐药是肿瘤患者死亡的主要原因。乙醛脱氢酶(ALDH)家族与肿瘤细胞的增殖、迁移、侵袭及耐药密切相关,不同的ALDH亚型在不同肿瘤细胞中表达。本研究旨在阐明人肺腺癌HCC-827/GR细胞(对吉非替尼耐药)中的ALDH亚型。
用人肺腺癌HCC-827细胞构建吉非替尼耐药的HCC-827/GR细胞;采用流式细胞术检测HCC-827及HCC-827/GR中ALDH亚型的表达;用100μmol/L二乙氨基苯甲醛(DEAB)处理HCC-827/GR细胞前后,通过MTT法分析其增殖能力及对吉非替尼的敏感性;采用实时定量PCR检测HCC-827细胞及HCC-827/GR细胞中ALDH亚型的mRNA表达水平。
与HCC-827细胞相比,HCC-827/GR细胞中ALDH的阳性率增加。100μmol/L DEAB处理后,HCC-827/GR细胞的增殖能力下降。与HCC-827细胞相比,HCC-827/GR细胞中ALDH1A1和ALDH1L1 mRNA的表达增加,但ALDH3B2表达下降。
ALDH可能作为检测肺腺癌细胞对吉非替尼耐药的分子生物标志物,且ALDH1A1可能在肺癌吉非替尼耐药中发挥作用。