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联合检测SATB2、CK20和CK7对结直肠癌病理诊断的价值 被引量:9

Diagnostic value of SATB2, CK7 and CK20 in colorectal cancer
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摘要 目的探讨联合检测SATB2、CK20及CK7在结直肠癌中的诊断价值。方法应用免疫组织化学法检测210例结直肠癌组织、100例非结直肠癌癌组织、90例肠癌淋巴结转移灶及50例正常结直肠黏膜中SATB2、CK20及CK7蛋白的表达情况。结果CK20+/CK7-联合检测诊断结直肠癌的灵敏度为78.1%,特异度为92.0%;CK20+/SATB2+/CK7-联合检测灵敏度为57.1%,特异度为98.0%;CK20+/CK7-或SATB2+/CK7-联合检测,灵敏度为85.7%,特异度为90.0%。结论联合检测CK20+/CK7-/SATB2+可提高结直肠癌诊断的特异度。在结直肠癌的诊断中,SATB2可作为一个重要的免疫组织化学补充检测指标。 Objective To study the diagnostic value of SATB2, together with CK7 and CK20, in colorectal cancer. Methods Immunohistochemical study for SATB2, CK7 and CK20 was carried out in 210 cases of colorectal cancer tissue, 100 cases of non-colorectal cancer tissue, 90 cases of lymph node metastases and 50 cases of normal colorectal mucosa. Results The sensitivity and specificity of CK20 +/ CK7 - immunophenotype for diagnosis of colorectal adenocarcinoma were 78. 1% and 92. 0% , respectively. When triple markers were used, the immunophenotype CK20 +/CK7 -/SATB2 + had a sensitivity of 57. 1% and a specificity of 98.0%. When combining the immunophenotype of SATB2 +/CK7 - or CK20 +/CK7-, the sensitivity was 85.7% and specificity was 90.0%. Conclusions A panel of immunohistochemical markers SATB2, CK7 and CK20 could increase the specificity for diagnosis of colorectal adenocarcinoma significantly. SATB2 is considered as a useful adjunct in this respect.
出处 《中华病理学杂志》 CAS CSCD 北大核心 2015年第8期578-581,共4页 Chinese Journal of Pathology
基金 国家自然科学基金(81171391) 苏州市科教兴卫青年科技项目(KJXW2013023)
关键词 结直肠肿瘤 SATB2 CK7 CK20 Colorectal neoplasms SATB2 CK7 CK20
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  • 1Dame MK, Jiang Y, Appelman HI), et al. Human colonic crypts in culture: segregation of immunochemical markers in normal versus adenoma-derived[J1. Lab Invest. 2014.94(2) : 222-234. 被引量:1
  • 2Tot T. Adenocarcinomas metastatic to the liver: the value of cytokeratins 20 and 7 in the search for unknown primary tumors []]. Cancer,1999,85(1 ) :171-177. 被引量:1
  • 3Chu P, Wu E, Weiss LM. Cytokeratin 7 and cytokeratin 20 expression in epithelial neoplasms: a survey of 435 cases[J]. Mod Pathol, 2000,13 (9) :962-972. 被引量:1
  • 4Dragomir A, de Wit M, Johansson C, et al. The role of SATB2 as a diagnostic marker for tumors of colorectal origin: results of a pathology-based clinical prospective study [ J ]. Am J Clin Pathol, 2014,141 (5) :630-638. 被引量:1
  • 5Dennis JL, Hvidsten TR, Wit EC, et al. Markers of adenocarcinoma characteristic of the site of origin : development of a diagnostic algorithm [ J ]. Clin Cancer Res, 2005,11 ( 10 ) : 3766-3772. 被引量:1
  • 6Bayrak R, Hahas H, Yenidunya S. The value of CDX2 and cytokeratins 7 and 20 expression in differentiating colorectal adenocarcinomas from extraintestinal gastrointestinal adenocarcinomas: cytokeratin 7 -/20 + phenotype is more specific than CDX2 antibody[ J]. Diagn Pathol, 2012,7:9. 被引量:1
  • 7Kim JH, Rhee YY, Bae ]M, et al. Loss of CDX2/CK20 expression is associated with poorly differentiated carcinoma, the CpG island methylator phenotype, and adverse prognosis in microsatellite-unstable colorectal cancer [ J]. Am J Surg Pathol, 2013. 37 (10) 1532-15ztl. 被引量:1
  • 8Yang MH, Yu J, Chen N, et al. Elevated microRNA-31 expression regulates colorectal cancer progression by repressing its target gene SATB2[J]. PLoS One, 2013, 8(12) :e85353. 被引量:1
  • 9Eberhard J, Gaber A, Wangefjord S, et al. A cohort study of the prognostic and treatment predictive value of SATB2 expression in colorectal cancer[ J]. Br J Cancer, 2012,106 (5) :931-938. 被引量:1
  • 10Gonner JR, Homick JL. SATB2 is a novel marker of osteoblastic differentiation in bone and soft tissue tumours[ J]. Histopathology, 2013, 63(1): 3649. 被引量:1

同被引文献47

  • 1余力,丁彦青,肖莎,赖飞菊,卢贤.结直肠癌CK7阳性表达的临床病理学意义[J].南方医科大学学报,2007,27(8):1190-1192. 被引量:4
  • 2Geller DS, Gorlick R. Osteosarcoma: a review of diagnosis, management, and treatment strategies [ J ]. Clin Adv Hematol Oncol,2010,8(10) :705-718. 被引量:1
  • 3Isakoff MS, Bielack SS, Meltzer P, et al. Osteosareoma: current treatment and a collaborative pathway to success[ J]. J Clin Oncol, 2015,33 (27) :3029-3035. DOI : 10. 1200/JCO. 2014.59. 4895. 被引量:1
  • 4Sheehan-Rooney K, Pflinka~ov6 B, Eberhart JK, et al. A cross- species analysis of Satb2 expression suggests deep conservation across vertebrate lineages [ J ]. Bey Dyn, 2010,239 ( 12 ) : 3481- 3491. DOI: 10. 1002/dvdy. 22483. 被引量:1
  • 5Dobreva G, Chahrour M, Dautzenberg M, et al. SATB2 is a muhifunctional determinant of craniofacial patterning and osteoblast differentiation [ J ]. Cell, 2006,125 (5) :971-986. 被引量:1
  • 6Gaspar N, Hawkins DS, Dirksen U, et al. Ewing sarcoma: current management and future approaches through collaboration [ J ]. J Clin Oneol, 2015,33 (27) : 3036-3046. DOI: 10. 1200/JCO. 2014.59. 5256. 被引量:1
  • 7Italiano A, Mir O, Ciofil A, et al. Advanced chondrosarcomas: role of chemotherapy and survival [ J ]. Ann Oncol, 2013,24 ( 11 ) : 2916-2922. DOI: 10. 1093/annonc/mdt374. 被引量:1
  • 8Li J, Zhang H, Yang C, et al. An overview of osteocalcin progress [J]. J Bone Miner Metab, 2016,In press. 被引量:1
  • 9Conner JR, Homick JL. SATB2 is a novel marker of osteoblastic differentiation in bone and soft tissue tumours [ J ]. Histopathology, 2013,63 ( 1 ) :36-49. DOI : 10.1111/his. 12138. 被引量:1
  • 10Righi A, Gambarotti M, Longo S, et al. Small cell osteosarcoma:clinicopatholngic, immunohistochemical, and molecular analysis of 36 cases[J]. Am J Surg Pathol, 2015,39(5):691-699. DOI: 10. 1097/PAS. 0000000000000412. 被引量:1

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