Annexin A10 expression in microsatelliteunstable colorectal cancers cancers: Is it specific to sporadic tumors?

American Journal of Surgical Pathology

Volumn 38, Issue 11, 2014, Pages 1577-1579

  Kim, Jung Ho ^a   Kang, Gyeong Hoon ^a  

^a Seoul National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ANNEXIN; TUMOR MARKER;

BIOSYNTHESIS; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; FEMALE; HUMAN; MALE;

ANNEXINS; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; FEMALE; HUMANS; MALE; TUMOR MARKERS, BIOLOGICAL;

EID: 84914812004     PISSN: 01475185     EISSN: 15320979     Source Type: Journal    
DOI: 10.1097/PAS.0000000000000306     Document Type: Letter

References (4)

1. Pai RK, Shadrach BL, Carver P, et al. Immunohistochemistry for annexin A10 can distinguish sporadic from lynch syndromeassociated microsatellite-unstable colorectal carcinoma. Am J Surg Pathol. 2014;38:518-525.
2. Kim JH, Rhee YY, Kim KJ, et al. Annexin A10 expression correlates with serrated pathway features in colorectal carcinoma with microsatellite instability. APMIS. 2014. [Epub ahead of print].
3. Geiersbach KB, Samowitz WS. Microsatellite instability and colorectal cancer. Arch Pathol Lab Med. 2011;135:1269-1277.
4. Capper D, Voigt A, Bozukova G, et al. BRAF V600E-specific immunohistochemistry for the exclusion of Lynch syndrome in MSI-H colorectal cancer. Int J Cancer. 2013;133:1624-1630.