[1]Laforest A, Aparicio T, Zaanan A, et al. ERBB2 gene as a potential therapeutic target in small bowel adenocarcinoma[J].Eur J Cancer,2014,50(10): 1740-1746.
[2]Overman MJ, Hu CY, Kopetz S, et al. A population-based comparison of adenocarcinoma of the large and small intestine: insights into a rare disease [J]. Ann Surg Oncol, 2012, 19(5):1439-1445.
[3]Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012[J]. CA Cancer J Clin, 2012, 62:10-29.
[4]Bennett CM, Coleman HG, Veal PG, et al. Lifestyle factors and small intestine adenocarcinoma risk: A systematic review and meta-analysis[J].Cancer Epidemiol, 2015, 39(3):265-273.
[5]Shenoy S. Genetic risks and familial associations of small bowel carcinoma [J]. World J Gastrointest Oncol, 2016, 8(6):509-519.
[6]Schrock AB, Devoe CE, Mcwilliams R, et al. Genomic profiling of small-bowel adenocarcinoma [J]. JAMA Oncol, 2017, 3(11):1546-1553.
[7]Jun SY, Lee EJ, Kim MJ, et al. Lynch syndrome-related small intestinal adenocarcinomas [J]. Oncotarget, 2017, 8(13): 21483-21500.
[8]Zhang YF, Mao XY, Zheng JC, et al. Small intestine adenocarcinoma associated with Peutz-Jeghers syndrome: a report of 5 cases and literature review [J]. J Clin Oncol, 2014, 13(7): 337-340.
[9]Svrcek M, Piton G, Cosnes J, et al. Small bowel adenocarcinomas complicating Crohn's disease are associated with dysplasia: a pathological and molecular study [J]. Inflamm Bowel Dis, 2014, 20(9):1584-1592.
[10]Aparicio T, Zaanan A, Svrcek M, et al. Small bowel adenocarcinoma: epidemiology, risk factors, diagnosis and treatment [J]. Digest Liver Dis, 2014, 46(2): 97-104.
[11]Goh AM, Xue Y, Leushacke M, et al. Mutant p53 accumulates in cycling and proliferating cells in the normal tissues of p53 R172H mutant mice [J]. Oncotarget, 2015, 6(20):17968-17980.
[12]Hsiao SJ, Remotti HE. Beta-catenin and p53 expression in ampullary and small intestinal adenocarcinoma [J]. J Clin Oncol, 2013, 31(15): e14659.
[13]Chen L, Wu T, Pathology DO. Elevation of Notch1- and P53-immunoreactivity in small intestinal adenocarcinoma[J]. Chin J Histochem Cytochem, 2016, 2:130-135.
[14] Pedersen LN, Krlev L, Teglbjrg PS, et al. Glutathione S -transferase genotype and p53 mutations in adenocarcinoma of the small intestine[J]. Scand J Gastroentero, 2003, 38(8):845-849.
[15]Gulhati P, Raghav K, Shroff RT, et al. Bevacizumab combined with capecitabine and oxaliplatin in patients with advanced adenocarcinoma of the small bowel or ampulla of vater: A single-center, open-label, phase 2 study[J]. Cancer, 2017, 123(6): 1011-1017.
[16]Freeman TJ, Smith JJ, Chen X, et al. Smad4-mediated signaling inhibits intestinal neoplasia by inhibiting expression of β-catenin[J]. Gastroenterol, 2012, 142(3): 562-571.
[17]郭文娟, 王爱英, 高春. 小肠腺癌组织的细胞凋亡及相关蛋白Bid和Bcl-xL的表达及意义[J]. 世界华人消化杂志, 2010, 18(11):1127-1133.
[18]Yang MC, Lin RW, Huang SB, et al. Bim directly antagonizes Bcl-xl in doxorubicin-induced prostate cancer cell apoptosis independently of p53 [J]. Cell Cycle, 2016, 15(3):394-402.
[19]Jun SY, Kim M, Gu MJ, et al. Clinicopathologic and prognostic associations of KRAS and BRAF mutations in small intestinal adenocarcinoma[J]. Mod Pathol, 2016, 29(4): 402-415.
[20]李小燕, 卢可, 张志,等. E-cadherin在小肠腺癌、小肠腺瘤中的表达及其意义[J]. 安徽医药, 2014,(11):2112-2114.
[21]Lee HJ, Lee OJ, Jang KT, et al. Combined loss of E-cadherin and aberrant β-Catenin protein expression correlates with a poor prognosis for small intestinal adenocarcinomas[J]. Am J Clin Patholo, 2013, 139(2):167-176.
[22]Alvi MA, Mcart DG, Paul K, et al. Comprehensive molecular pathology analysis of small bowel adenocarcinoma reveals novel targets with potential for clinical utility[J]. Oncotarget, 2015, 6(25):20863-20874.
[23]Overman MJ, Pozadzides J, Kopetz S, et al. Immunophenotype and molecular characterisation of adenocarcinoma of the small intestine [J]. Brit J Cancer, 2010, 102(1):144-150.
[24]高峰, 王小云, 卢加杰,等. 小肠腺癌微卫星不稳定与hMLH1和hMSH2基因突变相关性分析[J]. 中华肿瘤防治杂志, 2014, 21(9):688-691.
[25]Zaaimi Y, Aparicio T, Laurentpuig P, et al. Advanced small bowel adenocarcinoma: Molecular characteristics and therapeutic perspectives [J]. Clin Res Hepatol Gas, 2016, 40(2):154-160.
[26]Michel S, Kloor M, Singh S, et al. Coding microsatellite instability analysis in microsatellite unstable small intestinal adenocarcinomas identifies MARCKS as a common target of inactivation [J]. Mol Carcinogen, 2010, 49(2):175-182.
[27]Kim KJ, Kim JY, Hong SM, et al. Loss of CADM4 expression is associated with poor prognosis in small intestinal adenocarcinomas[J]. Apmis, 2017, 125(5): 437-443.
[28]吴婧婧, 顾康生. 小肠腺癌患者中MMP-9、Ki-67、EGFR和VEGF的表达与临床特征及预后的相关性研究[J]. 安徽医科大学学报, 2013, 48(6):647-651.
[29]吴晓华, 张莘, 周文阔. 原发性小肠腺癌中 PTEN 蛋白及 PCNA 的表达及临床意义[J]. 河北医药, 2014(3):330-332.
[30]Suzuki H, Hirata Y, Suzuki N, et al. Characterization of a new small bowel adenocarcinoma cell line and screening of anti-cancer drug against small bowel adenocarcinoma [J]. Am J Pathol, 2015, 185(2): 550-562.
[31]Zhang H, Zhang C. Expressions of filam in A and protein kinase B in small bowel adenocarcinoma and their significance[J].J Transl Med, 2016,1:14-18.
[32]Hare LM, Phesse TJ, Waring PM, et al. Physiological expression of the PI3K-activating mutation Pik3ca(H1047R) combines with Apc loss to promote development of invasive intestinal adenocarcinomas in mice[J]. Biochem J, 2014, 458(2):251-258.
[33]Janku F, Tsimberidou AM, Garridolaguna I, et al. PIK3CA mutations in patients with advanced cancers treated with PI3K/AKT/mTOR axis inhibitors [J]. Mol Cancer Ther, 2011, 10(3):558.
[34] Pedersen K, Smyrk TC, Harrington S, et al. Programmed death-ligand 1 (PD-L1) expression in small bowel adenocarcinomas (SBA)[J].J Clin Oncol,2015,33(15): 3619-3619.
[35]Thota R, Gonzalez RS, Berlin J, et al. Could the PD-1 pathway be a potential target for treating small intestinal adenocarcinoma [J]? Am J Clin Pathol, 2017, 148(3):208-214.
[36]Xu C, Hua H, Chen T, et al. PD-L1 is correlated with p53 expression in patients with lung adenocarcinoma[J]. Int J Clin Exp Pathol, 2017,10(3):2701-2711. |