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基因,ras

基因,ras的相关文献在1996年到2022年内共计105篇,主要集中在肿瘤学、分子生物学、基础医学 等领域,其中期刊论文102篇、专利文献87157篇;相关期刊61种,包括中华病理学杂志、国际检验医学杂志、医学临床研究等; 基因,ras的相关文献由454位作者贡献,包括奉典旭、张圣道、蒋渝等。

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论文:102 占比:0.12%

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论文:87157 占比:99.88%

总计:87259篇

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基因,ras

-研究学者

  • 奉典旭
  • 张圣道
  • 蒋渝
  • 金晶
  • 韩天权
  • 何杨
  • 傅建新
  • 刘训良
  • 刘铭球
  • 吴永芳
  • 期刊论文
  • 专利文献

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    • 阎臻; 付晓瑞; 李新敏; 崔珺
    • 摘要: 目的探讨Harvery鼠肉瘤病毒癌基因(HRAS)表达对宫颈癌细胞自噬及凋亡的作用及其机制。方法构建宫颈癌小鼠模型,苏木精-伊红(HE)染色验证小鼠模型构建是否成功。将宫颈癌Hela细胞分为4组,空白对照组(A组:不转染任何序列)、阴性对照组(B组:转染空载体质粒)、HRAS vector组(C组:转染HRAS过表达质粒)、si-HRAS组(D组:转染HRAS沉默质粒siRNA)。实时定量聚合酶链反应(qRT-PCR)和Western blot分别检测宫颈癌组织和细胞中HRAS、磷酸酶和张力蛋白同源物基因(PTEN)、自噬相关基因7(ATG7)、微管相关蛋白1轻链3(LC3)、Beclin1、BCL2关联X蛋白(bax)、TNF受体超家族成员6(Fas)和E-cadherin的mRNA和蛋白表达水平,流式细胞术检测转染各组细胞凋亡情况。结果HE染色结果显示宫颈癌小鼠造模成功。宫颈癌小鼠模型中HRAS呈高表达,PTEN表达下调(t=9.450~14.260,P<0.05)。细胞转染后HRAS vector组HRAS、bcl-2 mRNA和蛋白表达水平明显上升,PTEN、ATG7、LC3、Beclin1、bax、Fas和E-cadherin均呈低表达,细胞凋亡率明显下降(F=1.011~220.400,P<0.05);而si-HRAS组趋势相反(F=3.160~622.800,P<0.05)。结论HRAS基因表达下调可能通过激活PTEN信号通路促进小鼠宫颈癌细胞自噬和凋亡,抑制上皮间质转化,从而抑制宫颈癌的发生。
    • 中国临床肿瘤学会(CSCO)结直肠癌专家委员会
    • 摘要: 结直肠癌是目前我国发病率及死亡率最高的恶性肿瘤之一.随着精准医疗理念及对肿瘤相关分子标志物研究的逐年深入,合理的检测及应用结直肠癌相关分子标志物已经成为目前临床实践的重要部分.为了提高临床医师对结直肠癌分子标志物的了解及应用,中国临床肿瘤学会(CSCO)结直肠癌专家委员会组织相关领域专家,根据近年的国内外临床研究及实际诊疗经验,经专家组反复修改讨论,撰写了结直肠癌分子标志物临床检测的专家共识,旨在为临床医师提供参考及指导,为结直肠癌患者提供更加精准、有效的治疗.
    • 陈阳; 冉雯雯; 王璐; 宋瑶琳; 李广起; 邢晓明
    • 摘要: cqvip:目的探讨G蛋白信号调节蛋白1(GPSM1)在结直肠癌中的表达及意义。方法收集2015年4月—2016年4月青岛大学附属医院收治的150例原发性结直肠癌病人的石蜡组织样本及临床病理资料。采用免疫组织化学法检测GPSM1在结直肠癌组织及癌旁组织中的表达,采用实时荧光定量PCR法检测结直肠癌病人石蜡组织样本中KRAS和NRAS的突变情况;分析GPSM1在结直肠癌组织中表达水平与病人临床病理特征及预后的相关性。结果结直肠癌组织中GPSM1的表达水平明显高于癌旁组织(χ^(2)=102.938,P<0.001)。GPSM1在结直肠癌组织中的高表达与淋巴结转移(χ^(2)=5.429,P=0.020)及KRAS突变(χ^(2)=4.030,P=0.045)相关。生存分析结果显示,GPSM1高表达组结直肠癌病人的无病和总体生存期较GPSM1低表达组明显缩短(P=0.046、0.036)。结论GPSM1在结直肠癌组织中高表达,并且与病人不良预后相关,可作为预测结直肠癌转移的潜在生物学指标。
    • 白雪; 贺平
    • 摘要: 目的 筛选结肠直肠癌(CRC)中与鼠类肉瘤病毒癌基因K-RAS突变相关的基因间长链非编码RNA(lincRNA).方法 使用来自癌症基因组图谱(TCGA)的RNA-Seq和临床数据来鉴定CRC中与K-RAS突变相关的lincRNA.受试者工作特征(ROC)曲线分析差异表达的lincRNA与K-RAS野生型或突变型CRC 5年和10年生存率的关系,筛选关键的lincRNA.通过Kaplan-Meier生存曲线分析关键lincRNA表达对患者5年和10年生存率的影响,同时分析关键lincRNA与患者临床特征的关系.结果 共分析了585个癌组织和51个正常组织样品的RNA-Seq数据.从数据中获得6452个lincRNA,其中有85个上调,40个下调.筛选出12个在K-RAS突变CRC中差异表达的lincRNA,其中AL390719.2为具有K-RAS突变的关键lincRNA.生存分析结果显示,在K-RAS突变型中lincRNA AL390719.2表达与患者10年生存率(Log-rankχ2=10.740,HR=3.255,P=0.002)和5年生存率(Log-rankχ2=11.720,HR=3.142,P=0.001)有关,在K-RAS野生型中lincRNA AL390719.2表达与预后无关(10年:Log-rankχ2=1.400,HR=0.822,P=0.221;5年:Log-rankχ2=1.997,HR=0.774,P=0.086).高表达AL390719.2的患者临床分期较晚,容易出现淋巴结转移和远处转移.结论 lincRNA AL390719.2高表达与K-RAS突变型CRC的不良预后相关,可能是CRC新的预后标志物和治疗靶点.
    • 潘理会; 李育庄; 李春辉
    • 摘要: 目的探讨结直肠癌(colorectal cancer,CRC)中人类表皮生长因子受体2(human epidermal growth factor receptor 2,HER-2,又为C-erbB-2)基因与鼠类肉瘤病毒癌基因(Kirsten rat sarcoma viral oncogene,KRAS)突变情况及其与临床病理特征的关系。方法回顾性分析238例结直肠癌患者相关临床资料。采用荧光原位杂交(fluorescence in situ hybridization,FISH)法检测结直肠癌组织中的C-erbB-2扩增情况。采用荧光实时定量聚合酶链式反应(real time quantity polymerase chain reaction,qRT-PCR)法检测KRAS的突变情况,并分析其与临床病理特征之间的关系。结果结直肠癌中C-erbB-2总扩增率为1.7%(4/238),KRAS总突变率为36.9%(88/238)。C-erbB-2扩增在年龄、性别、肿瘤发生部位、组织学分型、分化程度、淋巴结转移、Duke's分期及浸润深度等方面比较,差异均无统计学意义(均P>0.05)。KRAS突变在淋巴结转移及Duke's分期方面比较,差异均具有统计学意义(均P<0.05)。C-erbB-2与KRAS二者表达无相关关系(r=0.086,P=0.184)。结论结直肠癌发生和发展过程中C-erbB-2扩增与KRAS突变无相关性,KRAS突变与淋巴结转移和Duke's分期有关。
    • Liu Xiaona; Tian Zhuang; Wei Xiaofei; Wang Quan; Zhang Jiaxin; Jin Meishan; Duan Xiumei
    • 摘要: Objective To analyze the concordance of KRAS, NRAS, BRAF and PIK3CA gene mutations detected in plasma and matched tumor tissues in colorectal cancer patients, in order to provide good evidences to support plasma could be a potential surrogate of tumor tissue for gene mutation test. Methods One hundred and seventy?five cases of colorectal cancer were collected at the First Hospital of Jilin University, from October 2016 to October 2017.There were 101 males and 74 females, their ages ranged from 28 to 85 years,with median age of 59 years. The KRAS, NRAS, BRAF and PIK3CA gene mutations in the plasma and paired tumor specimens of all patients were detected by next generation sequencing. Results The results of tissue samples test were gold standard. Comparison of the four genes showed that concordance rates between plasma and tissue samples were 81.1%(Kappa=0.543), 99.4%(Kappa=0.886), 99.4% (Kappa=0.886) and 97.7%(Kappa=0.714) respectively for KRAS, NRAS, BRAF and PIK3CA. The plasma detection rates of these genes were related to tumor stage(P=0.001), but not to gender(P=0.468) and age(P=1.000) of patients. Conclusions The study shows a high concordance of KRAS, NRAS, BRAF and PIK3CA gene mutations in plasma against mutation status in tumor tissue. In colorectal cancer, tumor tissue remains the best specimen for gene detection. However, patients from tumor tissue specimens cannot be obtained, especially those with advanced metastases, plasma can be used instead of tissue to detect the mutation status of KRAS, NRAS, BRAF and PIK3CA to guide targeted therapy.%目的 通过检测结直肠癌患者血浆与组织中KRAS、NRAS、BRAF及PIK3CA基因突变情况,分析血浆与组织基因突变检测结果的一致性,为血浆可替代组织进行基因突变检测提供依据.方法 收集2016年10月至2017年10月在吉林大学白求恩第一医院进行手术切除的结直肠癌及其相应的患者血浆标本175例,其中男性101例,女性74例;患者年龄28~85岁,中位年龄59岁.运用二代测序法分别对175例结直肠癌患者的血浆和对应肿瘤组织的KRAS、NRAS、BRAF及PIK3CA基因突变状态进行检测.结果 以组织样本检测结果为金标准,KRAS基因在血浆和组织检测一致率为81.1%(Kappa值=0.543),NRAS检测一致率为99.4%(Kappa值=0.886),BRAF检测一致率为99.4% (Kappa值=0.886),PIK3CA检测一致率为97.7%(Kappa值=0.714),结果一致性较好;血浆中基因突变检测阳性率与结直肠癌患者的分期有关(P=0.001),与性别(P=0.468)、年龄(P=1.000)均无关.结论血浆检测KRAS、NRAS、BRAF、PIK3CA基因突变与组织的一致性较好.虽然肿瘤组织仍是最佳的检测标本,但在结直肠癌患者无法获得肿瘤组织标本时,尤其是晚期已发生转移的患者,可考虑用血浆代替组织检测KRAS、NRAS、BRAF及PIK3CA的突变状态,用于指导患者的靶向治疗.
    • 郑兴征; 谷玉春; 金玉兰; 朱力; 吴秉铨; 詹阳; 马建慧; 徐汉武; 支文雪; 陈天宝; 秦旭颖; 王鹏; 张立红
    • 摘要: 目的 通过对子宫内膜黏液性上皮病变中的KRAS突变情况进行分析,探讨KRAS突变与子宫内膜黏液癌的相关性.方法 收集2015年7月至2017年10月首都医科大学附属北京妇产医院病理科诊断的子宫内膜黏液性上皮病变43例,不典型性子宫内膜增生症10例,子宫内膜样癌12例.从中性甲醛固定石蜡包埋组织中提取基因组DNA,聚合酶链反应(PCR)扩增KRAS第2、3号外显子,并进行毛细管电泳分析突变情况.应用Fisher确切概率法对各组中KRAS突变差异情况进行比较.结果 43例子宫内膜黏液性上皮病变患者年龄33~77岁,平均年龄(55.12±9.34)岁,中位年龄55岁.8例具有黏液分化的不伴细胞不典型性的子宫内膜增生症均未检出KRAS突变.不典型性子宫内膜增生症、子宫内膜样癌、不典型性子宫内膜增生症伴黏液分化、子宫内膜样癌伴黏液分化与黏液癌中存在KRAS突变,检出比例分别为1/10、1/12、4/11、6/15和8/9.黏液癌与子宫内膜样癌组(P<0.01)、子宫内膜样癌伴黏液分化组(P<0.05)相比,KRAS突变分布差异具有统计学意义.结论 不典型性子宫内膜增生症伴黏液分化、子宫内膜样癌伴黏液分化和黏液癌中存在KRAS高频突变,提示KRAS突变激活与子宫内膜黏液癌的发病机制密切相关.%Objective To investigate the frequency of KRAS mutation in mucinous epithelial lesions of the endometrium, and analyze the correlation between KRAS mutation and the clinicopathologic features. Methods The cohort included forty-three cases of mucinous epithelial lesions of the endometrium selected from July 2015 to October 2017 from Beijing Obstetrics and Gynecology Hospital, and 22 control cases. Genomic DNA was extracted from formalin-fixed paraffin-embedded tissue sections. Polymerase chain reaction amplification for KRAS exons 2 and 3 was performed, followed by sequencing using capillary electrophoresis. The Fisher exact test was used to compare the prevalence of KRAS mutation among the different groups. Results The patients′age ranged from 33 to 77 years [ mean ( 55. 12 ± 9. 34) years, median 55 years] . None of the eight cases of endometrial hyperplasia with mucinous differentiation without atypia showed KRAS mutation. The frequency of KRAS mutations was 1/10 in endometrial atypical hyperplasia, 1/12 in endometrioid carcinoma, 4/11 in endometrial atypical hyperplasia with mucinous differentiation ( EAHMD) , 6/15 in endometrioid carcinoma with mucinous differentiation ( ECMD) and 8/9 in mucinous carcinoma ( MC) , respectively. The differences were statistically significant between MC versus EC ( P<0. 01) and MC versus ECMD ( P<0. 05) . Conclusion The high frequency of KRAS mutation in EAHMD, ECMD and MC indicates that KRAS mutational activation is implicated in the pathogenesis of endometrial mucinous carcinoma.
    • 肖娜; 唐一通; 崔海忠; 李智山; 邹玖明
    • 摘要: 目的 研究一种简便、灵敏的K-ras基因突变检测方法,使其适合于进行常规突变检测.方法 设计对应检测位点寡核苷酸探针,经探针的连接、扩增、标记及ELISA反应,通过ELISA反应检测值确定突变位点基因型.以K-ras基因12位密码子的G12S、G12R、G12C、G12D、G12A、G12V 6个点突变为检测对象,对72例肺癌血浆循环DNA标本进行检测,并与直接测序结果进行比较.结果 利用建立方法共检出3例标本分别存在G12S、G12R、G12A突变.而通过直接测序未能从标本中检出K-ras突变,表明直接测序方法灵敏度较低,不适合于对循环DNA等不均一标本进行突变检测.结论 建立了一种简便、灵敏的K-ras基因突变检测方法,能够对不均一标本进行常规突变检测.%Objective To research a simple and sensitive K-ras gene mutations detection method in order to be suitable for the routine mutation detection.Methods The corresponding detection locus oligonucleotide probe was designed.By the connection,amplification,labeling and ELISA reaction in probe,the mutation locus genotype was determined by the ELISA reaction detection value.With the six point mutations of G12S,G12R,G12C,G12D,G12A and G12V in 12 codons of K-ras gene as the detection objects,the plasma circulation DNA sample in 72 cases of lung cancer was detected,then the results were compared with those obtained by the direct sequencing.Results Three samples were identified as the G12S,G12R and G12A mutatins by the established method.But no K-ras mutations were detected in the samples by using the direct sequencing,indicating that the direct sequencing had lower sensitivity and was not suitable for the mutation detection of heterogeneous samples such as circulating DNA.Conclusion The simple and sensitive K-ras gene mutation detection method is established and can conduct the routine mutation detection for the heterogeneous samples.
    • 夏丹丹; 王惠宇; 许隽颖; 刘超英
    • 摘要: 目的 分析不同部位大肠癌患者的K-ras基因突变状态与临床病理特征、预后情况的关系.方法 回顾性分析69例于2007年5月至2017年8月在南京医科大学附属无锡市人民医院经病理诊断为大肠癌并行K-ras基因检测患者的临床病理资料,分析其临床病理特征与K-ras基因突变状态的关系,随访预后情况,进行Kaplan-Meier生存分析.结果 69例大肠癌患者K-ras基因突变率为50.7%(35/69),其中,左、右半结肠癌和直肠癌患者分别为40.0%(12/30)、73.3%(11/15)、50.0%(12/24).年龄≥60岁、血清糖类抗原19-9(CA19-9)升高患者K-ras基因突变率分别较<60岁、血清CA19-9正常患者升高[61.5%(24/39)比36.7%(11/30),χ2=4.197,P=0.041;65.6%(19/29)比37.5%(15/40),χ2=5.486,P=0.019],而与患者性别、肿瘤原发部位、病理类型、TNM分期、血清癌胚抗原水平、临床症状等无关(均P>0.05).大肠癌患者K-ras基因突变与预后无关(χ2=0.001,P=0.997).K-ras基因状态与不同部位大肠癌患者总生存无关(χ2=0.583,P=0.445).左半结肠癌、直肠癌、右半结肠癌患者5年总生存率分别为76.9%、69.7%、31.3%,大肠癌原发部位与总生存有关(χ2=11.004,P=0.004).结论 大肠癌患者K-ras基因突变与年龄及血清CA19-9水平有关.左半结肠癌预后最佳,直肠癌次之,右半结肠癌最差.K-ras基因状态是否为大肠癌预后因素尚不明确.对大肠癌患者行K-ras基因、血清肿瘤标志物检测并明确发病部位、年龄层次,可为临床靶向治疗选择及患者生存状况判断提供依据.%Objective To analyze the correlation between K-ras gene mutation and clinicopathological characteristics and prognosis of colorectal cancer patients with different primary sites.Methods The clinical and pathological records of 69 patients who were pathologically confirmed as colorectal cancer and tested K-ras gene status at Wuxi People's Hospital Affiliated to Nanjing Medical University between May 2007 and August 2017 were adopted.The correlation between clinicopathological characteristics and prognosis of colorectal cancer patients with different primary sites and K-ras gene mutation status were retrospectively analyzed.And the patients were visited to adopt the prognosis data and perform the Kaplan-Meier survival analysis.Results The K-ras mutation rate was 50.7%(35/69),including 40.0%(12/30)in left-side colon cancer,73.3%(11/15)in right-side colon cancer and 50.0%(12/24)in rectal cancer.The mutation rate of K-ras gene in patients ≥ 60 years old [61.5%(24/39)vs.36.7%(11/30),χ2= 4.197,P = 0.041] or serum CA19-9 raising up abnormally was conspicuously high [65.6%(19/29)vs.37.5%(15/40),χ 2= 5.486,P =0.019].Other clinicopathological characteristics,such as gender,lesion location,histological classification,TNM stage,serum CEA expression,clinical features had no correlation with K-ras gene mutation status(all P> 0.05).And no relationship was found between prognosis and overall survival of colorectal cancer patients with different primary sites and K-ras gene mutation status(χ 2= 0.001,P = 0.997; χ 2= 0.583,P =0.445).In general,the 5-year survival rate of left-side colon cancer patients was highest(76.9%),followed by rectal cancer(69.7%),and right-side colon cancer was lowest(31.3%).The primary site of colorectal cancer was related to the overall survival of patients(χ2=11.004,P =0.004).Conclusions K-ras gene mutation in colorectal cancer is closely related to age and serum CA19-9 levels of the patients.The prognosis of left-side colon cancer is best,rectal cancer second,and right-side colon cancer poorest.Whether K-ras gene mutation is the prognostic factor of colorectal cancer is not clear.Testing the K-ras gene status and serum tumor index expression,distinguish the primary site and age group will provide the theory basis and promote the clinical targeted therapy and improve the survival of colorectal cancer patients.
    • 方平; 王沣
    • 摘要: 目的 探讨非小细胞肺癌(NSCLC)患者功能性驱动基因表皮生长因子受体(EGFR)、间变淋巴瘤激酶(ALK)、Kirsten鼠肉瘤病毒癌基因(KRAS)和B-Raf原癌基因丝氨酸/苏氨酸蛋白激酶(BRAF)基因的突变状况.方法 选择2009年1月至2016年6月安徽省铜陵市人民医院及安徽省立医院呼吸科、胸外科、肿瘤科诊治的经病理诊断为NSCLC患者,共203例(其中铜陵市人民医院117例,安徽省立医院86例),收集患者的外科手术肿瘤组织标本和淋巴结活检、肺穿刺活检、气管镜活检和胸腔积液沉渣标本,应用突变扩增阻滞系统(ARMS)进行EGFR、KRAS和BRAF基因突变检测和免疫组化法进行ALK基因分析,采用χ2检验分析基因的突变率及其与临床特征的关系.结果NSCLC患者EGFR、ALK、KRAS和BRAF基因的突变率分别为51.23%(104/203),4.88%(8/164),10.69%(17/159)和1.26%(2/159).EGFR基因阳性突变率女性组66.67%(58/87)高于男性组36.21%(42/116),腺癌组48.80%(81/166)高于鳞癌组33.33%(7/21),非吸烟组63.38%(90/142)高于吸烟组16.39%(10/61),差异有统计学意义(χ2=18.45,113.13,37.69;均P0.05).ALK基因突变状况与性别、病理类型、吸烟状态之间均差异无统计学意义(χ2=0.00,0.86,0.55;均P>0.05).KRAS基因突变状况与性别、病理类型、吸烟状态之间均差异无统计学意义(χ2=3.63,2.13,2.36;均P>0.05).此外BRAF基因突变均为男性、吸烟患者.检测中发现3例19,21外显子EGFR双突变;1例EGFR和ALK双突变.结论 NSCLC患者EGFR基因突变率最高,其次为KRAS、ALK、BRAF基因. EGFR基因突变以女性、不吸烟、腺癌为优势人群, EGFR与ALK双突变可共存.
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