Literature DB >> 17636009

Expression and characterization of a human carboxylesterase 2 splice variant.

Marissa A Schiel1, Scheri-lyn Green, Wilhelmina I Davis, Paresh C Sanghani, William F Bosron, Sonal P Sanghani.   

Abstract

CPT-11 [7-ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin or Irinotecan] is a carbamate prodrug that is activated in vivo by carboxylesterase (CES)-2 to SN-38 (7-ethyl-10-hydroxycamptothecin), a potent topoisomerase I inhibitor. There is high interindividual variation when CPT-11 is used in the treatment of colorectal cancer. Several splice variants of CES2 are reported in the expressed sequence tag database. Real-time polymerase chain reaction was used to determine the abundance of the CES2 and splice variant of human carboxylesterase 2 (CES2Delta(458-473)) transcripts in 10 paired samples of human tumor and normal colon tissue. The results showed that the CES2Delta(458-473) transcript accounts for an average of 6% of total CES2 transcripts in colon tissue, and there is large interindividual variation in CES2 expression in both tumor and normal colon samples. The carboxylesterase activity of the colon samples was determined by 4-methylumbelliferyl acetate hydrolysis assays and nondenaturing polyacrylamide gel electrophoresis followed by activity staining. Significant, positive correlations were found between CES2 expression levels and both measures of carboxylesterase activity. We cloned and expressed the CES2Delta(458-473) protein in Sf9 insect cells. The purification profiles and preliminary characterization of the CES2Delta(458-473) protein indicated that the expressed protein is folded and glycosylated like CES2. However, in vitro assays show that the CES2Delta(458-473) protein lacks 4-methylumbelliferyl acetate and irinotecan hydrolase activities. In conclusion, we found that the CES2Delta(458-473) protein is an inactive splice variant of CES2 and that its transcript is spliced at a relatively constant rate in tumor and normal colon tissue.

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Year:  2007        PMID: 17636009     DOI: 10.1124/jpet.107.127027

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  6 in total

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2.  Enhancement of Dissolution Rate and Intestinal Stability of Clopidogrel Hydrogen Sulfate.

Authors:  Dina E Bali; Mohamed A Osman; Gamal M El Maghraby
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2016-12       Impact factor: 2.441

3.  Carboxylesterase 2 as a Determinant of Response to Irinotecan and Neoadjuvant FOLFIRINOX Therapy in Pancreatic Ductal Adenocarcinoma.

Authors:  Michela Capello; Minhee Lee; Hong Wang; Ingrid Babel; Matthew H Katz; Jason B Fleming; Anirban Maitra; Huamin Wang; Weihua Tian; Ayumu Taguchi; Samir M Hanash
Journal:  J Natl Cancer Inst       Date:  2015-05-29       Impact factor: 13.506

4.  Human carboxylesterase 2: Studies on the role of glycosylation for enzymatic activity.

Authors:  Márcia Alves; Joana Lamego; Tiago Bandeiras; Rute Castro; Hélio Tomás; Ana Sofia Coroadinha; Júlia Costa; Ana Luisa Simplício
Journal:  Biochem Biophys Rep       Date:  2015-11-19

Review 5.  Human carboxylesterases and fluorescent probes to image their activity in live cells.

Authors:  Anchal Singh; Mingze Gao; Michael W Beck
Journal:  RSC Med Chem       Date:  2021-05-18

6.  CES2, ABCG2, TS and Topo-I primary and synchronous metastasis expression and clinical outcome in metastatic colorectal cancer patients treated with first-line FOLFIRI regimen.

Authors:  Nicola Silvestris; Giovanni Simone; Giulia Partipilo; Emanuela Scarpi; Vito Lorusso; Anna Elisabetta Brunetti; Evaristo Maiello; Angelo Paradiso; Anita Mangia
Journal:  Int J Mol Sci       Date:  2014-09-05       Impact factor: 5.923

  6 in total

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