Literature DB >> 26124368

Maspin, a Marker of Serrated Colorectal Polyps.

Carlos A Rubio1, Ann Kaufeldt2, Jan Björk3, Edgar Jaramillo4.   

Abstract

The serine proteinase inhibitor maspin is a tumor-suppressor protein that stimulates apoptosis and inhibits motility, invasion and cancer metastasis. Mutant maspin galvanises partial loss of tumor-suppressor function, reducing susceptibility to apoptosis and facilitating malignant progression. Mutant maspin has been reported in many tumor types. We recently analyzed maspin expression in 128 colorectal lesions: 39 hyperplastic polyps (HPs), 29 sessile serrated adenoma/polyps (SSA/Ps), three traditional serrated adenomas (TSAs), 20 conventional colorectal adenomas (CCRAs), 5 carcinomas evolving from CCRA, 12 active inflammatory bowel disease (IBD), 2 ulcerative colitis (UC) in remission, 4 solitary ulcers (rectum) and 12 normal colorectal mucosa. The topographic distribution of maspin in the cytoplasm was classified into i) extensive, ii) focal, or iii) negative. The intensity of maspin expression in the cytoplasm was classified into i) unquestionable or ii) negative. Cases with faint (questionable) maspin expression were also recorded as negative. Extensive maspin expression was recorded in 95% (39/41) of the HPs, in 100% (29/29) of the SSA/Ps (including one carcinoma arising in a SSA/P), in 66% (2/3) of the TSAs, but only in 10% (2/20) of the CCRAs. None of the specimens with carcinoma arising in CCRA, with UC in remission or with solitary ulcer exhibited extensive maspin expression. Importantly, maspin was not expressed in the normal mucosa (including that adjacent to HP, SSA/P, TSA and CCRA). It is submitted that extensive maspin expression might be a manifestation of mutant maspin in lesions central to the serrated pathway of colorectal carcinogenesis. Copyright
© 2015 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.

Entities:  

Keywords:  Maspin; colon; conventional adenomas; rectum; serrated polyps

Mesh:

Substances:

Year:  2015        PMID: 26124368

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  3 in total

1.  Proteomic profiling of antibody-inducing immunogens in tumor tissue identifies PSMA1, LAP3, ANXA3, and maspin as colon cancer markers.

Authors:  Qian Yang; Michael H Roehrl; Julia Y Wang
Journal:  Oncotarget       Date:  2017-12-22

2.  Proteomic profiling identifies markers for inflammation-related tumor-fibroblast interaction.

Authors:  Daniel Drev; Andrea Bileck; Christopher Gerner; Brigitte Marian; Zeynep N Erdem; Thomas Mohr; Gerald Timelthaler; Andrea Beer
Journal:  Clin Proteomics       Date:  2017-10-06       Impact factor: 3.988

Review 3.  Subcellular Expression of Maspin in Colorectal Cancer: Friend or Foe.

Authors:  Simona Gurzu; Ioan Jung
Journal:  Cancers (Basel)       Date:  2021-01-20       Impact factor: 6.639

  3 in total

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