• 1.河北省衡水市哈勵遜國際和平醫(yī)院普外科(河北衡水 053000);;
  • 2.河北醫(yī)科大學第二醫(yī)院普外科(河北石家莊 050017);

目的  探討尾型同源盒轉錄因子-2 (CDX-2)和抑癌基因KAI-1在結腸癌中的表達并分析其臨床意義。
方法  應用免疫組織化學SP法檢測50例結腸癌組織及相應癌旁組織和25例正常結腸黏膜組織中CDX-2和KAI-1蛋白的表達,分析其表達與結腸癌患者臨床病理特征的關系以及二者表達的相關性。
結果 ?、僭诮Y腸癌組織及相應癌旁組織(距癌組織≤2cm)和正常結腸黏膜組織中CDX-2蛋白表達陽性率分別為34% (17/50)、54% (27/50)及88% (22/25),KAI-1蛋白表達陽性率分別為30% (15/50)、58% (29/50)及92% (23/25),CDX-2 和KAI-1在結腸癌組織中的蛋白表達陽性率均分別明顯低于相應癌旁組織(P<0.05)及正常結腸黏膜組織(P<0.05),其在癌旁組織中的表達陽性率也均明顯低于正常結腸黏膜組織(P<0.05)。②CDX-2和KAI-1蛋白表達陽性率與結腸癌淋巴結轉移、浸潤深度及分化程度均有關(P<0.05),即在有淋巴結轉移、浸潤深度浸及漿膜及分化程度較低者中CDX-2和KAI-1蛋白表達陽性率均明顯低于其在無淋巴結轉移、浸潤深度未及漿膜及分化程度較高者(P<0.05),二者均與患者的發(fā)病年齡和性別無關(P>0.05)。③Spearman等級相關分析表明,CDX-2和KAI-1蛋白陽性表達呈正相關(rs=0.544,P<0.01)。
結論  CDX-2和KAI-1的表達可能與結腸癌的發(fā)生、發(fā)展、浸潤、轉移及預后相關,聯(lián)合評價其功能可能對結腸癌治療具有一定指導意義。

引用本文: 劉繼攀,尹長恒,宋默,閻慶輝. CDX-2和KAI-1在結腸癌中的表達及臨床意義. 中國普外基礎與臨床雜志, 2013, 20(11): 1263-1267. doi: 復制

版權信息: ?四川大學華西醫(yī)院華西期刊社《中國普外基礎與臨床雜志》版權所有,未經(jīng)授權不得轉載、改編

1. Walsha T, Casadeia S, Ming K, et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing[J]. PNAS, 2011,108,(44):18032-18037.
2. Kang H, Chen IM, Wilson CS, et al. Gene expression classifiersfor relapse-free survival and minimal residual disease improve riskclassification and outcome prediction in pediatric B-precursor acutelymphoblastic leukemia[J]. Blood, 2010, 115(7):1394-1405.
3. Saad RS, Ismiil N, Dubé V, et al. CDX-2 expression is a commonevent in primary intestinal-type rndocervical adenocarcinoma[J].Am J Clin Pathol, 2009, 132(4):531-538.
4. Kenneth EH, Marco AM, Larissa GR, et al. Development of a mouse model for sporadic and metastatic colon tumors and its use in assessing drug treatment[J]. PNAS, 2010, 107(4):1565-1570.
5. Malik FA, Sanders AJ, Kayan MA, et al. Effect of expressional alteration of Kai1 on breast cancer cell growth, adhesion, migration and invasion[J]. Cancer Genomics Proteomics, 2009, 6(4):205-213.
6. Wei X, Li KC. Exploring the within- and between-class correlationdistributions for tumor classification[J]. Proc Natl Acad Sci, 2010, 7(15):6737-6742.
7. 于秀文, 榮瑋, 孫玉榮, 等. MUC2、CDX2在大腸腫瘤中的表達及臨床意義[J]. 中國現(xiàn)代醫(yī)學雜志, 2008, 18(21):3115-3119.
8. 許良中, 楊文濤. 免疫組織化學反應結果的判斷標準[J]. 中國癌癥雜志, 1996, 6(4):229-231.
9. Gross I, Duluc I, Benameur T, et al. The intestine-specific hom-eobox gene Cdx2 decreases mobility and antagonizes dissemination of colon cancer cells[J]. Oncogene, 2008, 27(1):107-115.
10. Mallo GV, Rechreche H, Frigerio JM, et al. Molecular cloning, sequencing and expression of the mRNA encoding human Cdx1 and Cdx2 homeobox. Down-regulation of Cdx1 and Cdx2 mRNA expression during colorectal carcinogenesis[J]. Int J Cancer, 1997, 74(1):35-44.
11. Sivagnanasundaram S, Islam I, Talbot I, et al. The homeobox gene CDX2 in colorectal carcinoma: a genetic analysis[J]. Br J Cancer, 2001, 84(2):218-225.
12. Qualtrough D, Hinoi T, Fearon E, et al. Expression of CDX2 in normal and neoplastic human colon tissue and during differentiation of an in vitro model system[J]. Gut, 2002, 51(2): 184-190.
13. Kaimaktchiev V, Terracciano L, Tornillo L, et al. The homeoboxintestinal differentiation factor CDX2 is selectively expressed ingastrointestinal adenocarcinomas[J]. Mod Pathol, 2004, 17(11):.
14. Drummond F, Sowden J, Morrison K, et al. The caudal-typehomeobox protein Cdx-2 binds to the colon promoter of the carbonicanhydrase 1 gene[J]. Eur J Biochem, 1996, 236(2): 670-681.
15. Sho M, Adachi M, Taki T, et al. Transmembrane 4 superfamily as a prognostic factor in pancreatic cancer[J]. Int J Cancer, 1998, 79(5):509-516.
16. Yang X, Welch DR, Phillips KK, et al. KAI1, a putative markerfor metastatic potential in human breast cancer[J]. Cancer Lett, 1997, 119(2):149-155.
17. Dong JT, Suzuki H, Pin SS, et al. Down-regulation of the KAI1 metastasis suppressor gene during the progression of human prostatic cancer infrequently involves gene mutation or allelic loss[J]. Cancer Res, 1996, 56(19): 4387-4390.
18. White A, Lamb PW, Barrett JC. Frequent downregulation of the KAI1(CD82) metastasis suppressor protein in human cancer cell lines[J]. Oncogene, 1998, 16(24):3143-3149.
19. Liu FS, Dong JT, Chen JT, et al. KAI1 metastasis suppressor protein is down-regulated during the progression of human endometrial cancer[J]. Clin Cancer Res, 2003, 9(4):1393-1398.
20. -1399.
  1. 1. Walsha T, Casadeia S, Ming K, et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing[J]. PNAS, 2011,108,(44):18032-18037.
  2. 2. Kang H, Chen IM, Wilson CS, et al. Gene expression classifiersfor relapse-free survival and minimal residual disease improve riskclassification and outcome prediction in pediatric B-precursor acutelymphoblastic leukemia[J]. Blood, 2010, 115(7):1394-1405.
  3. 3. Saad RS, Ismiil N, Dubé V, et al. CDX-2 expression is a commonevent in primary intestinal-type rndocervical adenocarcinoma[J].Am J Clin Pathol, 2009, 132(4):531-538.
  4. 4. Kenneth EH, Marco AM, Larissa GR, et al. Development of a mouse model for sporadic and metastatic colon tumors and its use in assessing drug treatment[J]. PNAS, 2010, 107(4):1565-1570.
  5. 5. Malik FA, Sanders AJ, Kayan MA, et al. Effect of expressional alteration of Kai1 on breast cancer cell growth, adhesion, migration and invasion[J]. Cancer Genomics Proteomics, 2009, 6(4):205-213.
  6. 6. Wei X, Li KC. Exploring the within- and between-class correlationdistributions for tumor classification[J]. Proc Natl Acad Sci, 2010, 7(15):6737-6742.
  7. 7. 于秀文, 榮瑋, 孫玉榮, 等. MUC2、CDX2在大腸腫瘤中的表達及臨床意義[J]. 中國現(xiàn)代醫(yī)學雜志, 2008, 18(21):3115-3119.
  8. 8. 許良中, 楊文濤. 免疫組織化學反應結果的判斷標準[J]. 中國癌癥雜志, 1996, 6(4):229-231.
  9. 9. Gross I, Duluc I, Benameur T, et al. The intestine-specific hom-eobox gene Cdx2 decreases mobility and antagonizes dissemination of colon cancer cells[J]. Oncogene, 2008, 27(1):107-115.
  10. 10. Mallo GV, Rechreche H, Frigerio JM, et al. Molecular cloning, sequencing and expression of the mRNA encoding human Cdx1 and Cdx2 homeobox. Down-regulation of Cdx1 and Cdx2 mRNA expression during colorectal carcinogenesis[J]. Int J Cancer, 1997, 74(1):35-44.
  11. 11. Sivagnanasundaram S, Islam I, Talbot I, et al. The homeobox gene CDX2 in colorectal carcinoma: a genetic analysis[J]. Br J Cancer, 2001, 84(2):218-225.
  12. 12. Qualtrough D, Hinoi T, Fearon E, et al. Expression of CDX2 in normal and neoplastic human colon tissue and during differentiation of an in vitro model system[J]. Gut, 2002, 51(2): 184-190.
  13. 13. Kaimaktchiev V, Terracciano L, Tornillo L, et al. The homeoboxintestinal differentiation factor CDX2 is selectively expressed ingastrointestinal adenocarcinomas[J]. Mod Pathol, 2004, 17(11):.
  14. 14. Drummond F, Sowden J, Morrison K, et al. The caudal-typehomeobox protein Cdx-2 binds to the colon promoter of the carbonicanhydrase 1 gene[J]. Eur J Biochem, 1996, 236(2): 670-681.
  15. 15. Sho M, Adachi M, Taki T, et al. Transmembrane 4 superfamily as a prognostic factor in pancreatic cancer[J]. Int J Cancer, 1998, 79(5):509-516.
  16. 16. Yang X, Welch DR, Phillips KK, et al. KAI1, a putative markerfor metastatic potential in human breast cancer[J]. Cancer Lett, 1997, 119(2):149-155.
  17. 17. Dong JT, Suzuki H, Pin SS, et al. Down-regulation of the KAI1 metastasis suppressor gene during the progression of human prostatic cancer infrequently involves gene mutation or allelic loss[J]. Cancer Res, 1996, 56(19): 4387-4390.
  18. 18. White A, Lamb PW, Barrett JC. Frequent downregulation of the KAI1(CD82) metastasis suppressor protein in human cancer cell lines[J]. Oncogene, 1998, 16(24):3143-3149.
  19. 19. Liu FS, Dong JT, Chen JT, et al. KAI1 metastasis suppressor protein is down-regulated during the progression of human endometrial cancer[J]. Clin Cancer Res, 2003, 9(4):1393-1398.
  20. 20. -1399.