参考文献/References:
[1]Butz ES,Chandrachud U,Mole SE,et al.Moving towards a new era of genomics in the neuronal ceroid lipofuscinoses[J].Biochim Biophys Acta Mol Basis Dis,2020,1866(9):165571.[2]杨兰,刘杰.Allo-HSCT治疗急性淋巴细胞白血病对患者近远期疗效和BCL6、NCL基因表达的影响探究[J].标记免疫分析与临床,2018,25(9):1372-1376.[3]Jamroziak K,Mlynarski W,Balcerczak E,et al.Functional C3435T polymorphism of MDR1 gene: an impact on genetic susceptibility and clinical outcome of childhood acute lymphoblastic leukemia[J].Eur J Haematol,2004,72(5):314-321.[4]赵富磊,李骞,柳汝明,等.ABCB1基因C3435T多态性与儿童急性淋巴细胞白血病相关性的分析[J].中国临床药理学杂志,2018,34(18):2224-2227.[5]Couto AC,Ferreira JD,Pombo-de-Oliveira MS,et al.maternal exposure to analgesic medicines, and leukemia in Brazilian children below 2 years of age[J].Eur J Cancer Prev,2015,24(3):245-252.[6]Zhou L,Chen W,Cao C,et al.Design and synthesis of α-naphthoflavone chimera derivatives able to eliminate cytochrome P450 (CYP)1B1-mediated drug resistance via targeted CYP1B1 degradation[J].Eur J Med Chem,2020(189):112028.[7]沈莉菁,陈芳源,王婷,等.CYP3A5基因多态性及其在急性白血病患者化疗与预后中的意义[J].中国实验血液学杂志,2008,16(1):26-30.[8]刘爽,曹流.细胞自噬相关基因Atg7与p53的协同作用对肿瘤发生发展的影响[D].沈阳:中国医科大学,2014.[9]杨秀丽,唐庆华,于洋.自噬基因ATG7、ATG12在成人急性淋巴细胞白血病骨髓单个核细胞中的表达及意义[J].武汉大学学报(医学版),2019,40(2):239-242.[10]Mortensen M,Soilleux EJ,Djordjevic G,et al.The autophagy protein Atg7 isessential for hematopoietic stem cell maintenance[J].J Exp Med,2011,208(3):455-467.[11]Rosales-Rodríguez B,Fernández-Ramírez F,Núnez-Enríquez JC,et al.Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia[J].Arch Med Res,2016,47(8):706-711.[12]何文华.急性淋巴细胞白血病患者ROCK1基因表达水平变化及其临床意义[J].中国实验血液学杂志,2019,27(2):415-420.[13]Kotwal J,Manoj MG,Kapoor R.Detection of balanced translocations in acute lymphoblastic leukemia by a novel multiplex reverse transcriptase reverse transcription-polymerase chain reaction[J].J Cancer Res Ther,2017,13(6):1042-1046.[14]Mei Y,Li Z,Zhang Y,et al.Low miR-210 and CASP8AP2 expression is associated with a poor outcome in pediatric acute lymphoblastic leukemia[J].Oncol Lett,2017,14(6):8072-8077.[15]Kamimura N,Goto T,Takahashi K,et al.A bacterial aromatic aldehyde dehydrogenase critical for the efficient catabolism of syringaldehyde[J].Sci Rep,2017(7):44422.[16]Sato K,Sakai H,Saiki Y,et al.Cell dynamics during differentiation therapy with all-trans retinoic acid in acute promyelocytic leukemia[J].Int J Hematol,2018,108(3):274-281.[17]Satar NA,Fakiruddin KS,Lim MN,et al.Novel triple positive markers identified in human non small cell lung cancer cell line with chemotherapy-resistant and putative cancer stem cell characteristics[J].Oncol Rep,2018,40(2):669-681.[18]刘雨薇,曲艺,颜晓菁.ALDH3B1在急性淋巴细胞白血病中的表达及意义[J].中国医科大学学报,2019,48(10):896-900.[19]Broxmeyer HE,Mor-Vaknin N,Kappes F,et al.Concise review: role of DEK in stem/progenitor cell biology[J].Stem Cells,2013,31(8):1447-1453.[20]石玉.SET/CAN和DEK/CAN融合基因阳性急性髓系白血病一例并文献复习[J].白血病·淋巴瘤,2017,26(11):692-694.[21]赵霄晨,何苗,白海.伴DEK-CAN融合基因阳性急性髓系白血病二例并文献复习[J].海南医学,2018,29(23):3395-3397.[22]Oancea C,Rüster B,Brill B,et al.STAT activation status differentiates leukemogenic from non-leukemogenic stem cells in AML and is suppressed by arsenic in t(6;9)-positive AML[J].Genes Cancer,2014,5(11-12):378-392.[23]Sun Z,Terragni J,Borgaro JG,et al.High-resolution enzymatic mapping of genomic 5-hydroxymethylcytosine in mouse embryonic stem cells[J].Cell Rep,2013,3(2):567-576.[24]Magotra M,Sakhdari A,Lee PJ,et al.Immunohistochemical loss of 5-hydroxymethylcytosine expression in acute myeloid leukaemia: relationship to somatic gene mutations affecting epigenetic pathways[J].Histopathology,2016,69(6):1055-1065.[25]Rakowski LA,Lehotzky EA,Chiang MY.Transient responses to NOTCH and TLX1/HOX11 inhibition in T-cell acute lymphoblastic leukemia/lymphoma[J].PLoS One,2011,6(2):e16761.[26]Collins CT,Hess JL.Role of HOXA9 in leukemia: dysregulation, cofactors and essential targets[J].Oncogene,2016,35(9):1090-1098.[27]Pan MM,Zhang QY,Wang YY,et al.Human NUP98-IQCG fusion protein induces acute myelomonocytic leukemia in mice by dysregulating the Hox/Pbx3 pathway[J].Leukemia,2016,30(7):1590-1593.[28]Zhang X,Liang X,Gu J,et al.Investigation and intervention of autophagy to guide cancer treatment with nanogels[J].Nanoscale,2017,9(1):150-163.[29]Liang B,Wang J.EVI1 in Leukemia and Solid Tumors[J].Cancers(Basel),2020,12(9):2667.[30]刘云峰,王林,杨碧珊,等.EVI1高表达AML的潜在治疗新靶点GNGT2[J].基因组学与应用生物学,2019,38(10):4763-4768.[31]Will B,Vogler TO,Narayanagari S,et al.Minimal PU.1 reduction induces a preleukemic state and promotes development of acute myeloid leukemia[J].Nat Med,2015,21(10):1172-1181.[32]Benekli M,Xia Z,Donohue KA,et al.Constitutive activity of signal transducer and activator of transcription 3 protein in acute myeloid leukemia blasts is associated with short disease-free survival[J].Blood,2002,99(1):252-257.[33]Luo HM,Wu X,Xian X,et al.Calcitonin gene-related peptide inhibits angiotensin II-induced NADPH oxidase-dependent ROS via the Src/STAT3 signalling pathway[J].J Cell Mol Med,2020,24(11):6426-6437.[34]Dimri S,Malhotra R,Shet T,et al.Noncanonical pS727 post translational modification dictates major STAT3 activation and downstream functions in breast cancer[J].Exp Cell Res,2020,396(2):112313.[35]黄成双,谭梅,张相梅,等.STAT3基因在急性髓系白血病中的表达及临床意义[J].中国实验血液学杂志,2019,27(1):45-51.[36]李光曦,张军,靳小可,等.RNA干扰HuR基因表达对急性髓系白血病细胞凋亡和CD7、CD19表达的影响及机制研究[J].广西医科大学学报,2018,35(8):1046-1049.[37]Gromova I,Gromov P,Kroman N,et al.Immunoexpression analysis and prognostic value of BLCAP in breast cancer[J].PLoS One,2012,7(9):e45967.[38]Slattery ML,Herrick JS,Pellatt DF,et al.MicroRNA profiles in colorectal carcinomas, adenomas and normal colonic mucosa: variations in miRNA expression and disease progression[J].Carcinogenesis,2016,37(3):245-261.[39]黄凤霞,李海燕,苏媛媛,等.miRNA-107在急性髓系白血病中的表达及意义[J].标记免疫分析与临床,2019,26(12):1988-1993.[40]Kitagishi Y,Matsuda S.Redox regulation of tumor suppressor PTEN in cancer and aging (Review)[J].Int J Mol Med,2013,31(3):511-515.[41]孙巨勇,牟娜,牟佳,等.PTEN及BCL-2在急性髓系白血病中的表达及意义[J].中国实验血液学杂志,2018,26(1):121-125.[42]Liu H,Chen C,Ma D,et al.Inhibition of PIM1 attenuates the stem cell-like traits of breast cancer cells by promoting RUNX3 nuclear retention[J].J Cell Mol Med,2020,24(11):6308-6323.[43]周震沧,田祖国,袁钟.Pim-3基因在急性髓系白血病中的表达及意义[J].中国实验血液学杂志,2016,24(2):316-320.
相似文献/References:
[1]李瑞珍,张月荣.完全缓解急性白血病脑脊液检出白血病细胞的检验分析[J].医学信息,2018,31(06):146.[doi:10.3969/j.issn.1006-1959.2018.06.051]
LI Rui-zhen,ZHANG Yue-rong.Detection and Analysis of Leukemic Cells in Cerebrospinal Fluid for Complete Remission of Acute Leukemia[J].Medical Information,2018,31(20):146.[doi:10.3969/j.issn.1006-1959.2018.06.051]
[2]王东梅,张展英.小细胞肺癌中信号通路及蛋白相互作用网络分析[J].医学信息,2020,33(01):81.[doi:10.3969/j.issn.1006-1959.2020.01.025]
WANG Dong-mei,ZHANG Zhan-ying.Analysis of Signal Pathways and Protein Interaction Networks in Small Cell Lung Cancer[J].Medical Information,2020,33(20):81.[doi:10.3969/j.issn.1006-1959.2020.01.025]
[3]周 莛,朱 岷.儿童肾上腺危象临床特征及基因分析[J].医学信息,2020,33(09):67.[doi:10.3969/j.issn.1006-1959.2020.09.020]
ZHOU Ting,ZHU Min.Clinical Characteristics and Genetic Analysis of Children’s Adrenal Crisis[J].Medical Information,2020,33(20):67.[doi:10.3969/j.issn.1006-1959.2020.09.020]
[4]吴 思,邢巍巍.辽西地区非综合征性耳聋患者及其亲属常见耳聋基因检测结果分析[J].医学信息,2020,33(11):122.[doi:10.3969/j.issn.1006-1959.2020.11.038]
WU Si,XING Wei-wei.Analysis of Common Deafness Gene Detection Results in Non-syndromic Deafness Patients and Their Relatives in Western Liaoning[J].Medical Information,2020,33(20):122.[doi:10.3969/j.issn.1006-1959.2020.11.038]
[5]谌玉佳,杨江涛,庄利明,等.深圳市光明区新生儿耳聋基因筛查结果分析[J].医学信息,2020,33(13):134.[doi:10.3969/j.issn.1006-1959.2020.13.039]
CHEN Yu-jia,YANG Jiang-tao,ZHUANG Li-ming,et al.Analysis of Genetic Screening Results of Newborn Deafness in Guangming District,Shenzhen[J].Medical Information,2020,33(20):134.[doi:10.3969/j.issn.1006-1959.2020.13.039]
[6]郑 珊,刘雪静,田秀英.MTM1基因突变致新生儿中央核性肌病2例[J].医学信息,2021,34(06):191.[doi:10.3969/j.issn.1006-1959.2021.06.054]
[7]吴文钦,熊戌霞,蔡梦珊.深圳市龙华区地中海贫血基因分型情况分析[J].医学信息,2021,34(14):142.[doi:10.3969/j.issn.1006-1959.2021.14.039]
WU Wen-qin,XIONG Xu-xia,CAI Meng-shan.Analysis on the Genotyping of Thalassemia in Longhua District,Shenzhen[J].Medical Information,2021,34(20):142.[doi:10.3969/j.issn.1006-1959.2021.14.039]
[8]魏谭伟.先天性无虹膜症PAX6致病基因分析及其分子诊断研究[J].医学信息,2022,35(10):78.[doi:10.3969/j.issn.1006-1959.2022.10.019]
WEI Tan-wei.A PAX6 Pathogenic Gene Analysis and Molecular Diagnosis of Congenital Aniridia[J].Medical Information,2022,35(20):78.[doi:10.3969/j.issn.1006-1959.2022.10.019]
[9]吴玉斌,李先明.涎腺粘液表皮样癌与腺样囊性癌基因突变及靶向治疗研究[J].医学信息,2022,35(11):64.[doi:10.3969/j.issn.1006-1959.2022.11.018]
WU Yu-bin,LI Xian-ming.Study on Gene Mutation and Targeted Therapy of Mucoepidermoid Carcinoma and Adenoid Cystic Carcinoma of Salivary Gland[J].Medical Information,2022,35(20):64.[doi:10.3969/j.issn.1006-1959.2022.11.018]
[10]符青云,欧阳小明,郅 程,等.结直肠癌组织EGFR、BRAF及NRAS基因突变检测及临床意义分析[J].医学信息,2022,35(13):83.[doi:10.3969/j.issn.1006-1959.2022.13.018]
FU Qing-yun,OUYANG Xiao-ming,ZHI Cheng,et al.Detection and Clinical Significance of EGFR, BRAF and NRAS Gene Mutations in Colorectal Cancer[J].Medical Information,2022,35(20):83.[doi:10.3969/j.issn.1006-1959.2022.13.018]