Literature DB >> 10475619

A colorimetric assay to evaluate the chemotherapeutic response of children with acute lymphoblastic leukemia (ALL) employing achatininH: a 9-O-acetyl sialic acid binding lectin.

D Sinha1, D K Bhattacharya, C Mandal.   

Abstract

Employing a 9-O-acetyl sialic acid binding lectin, Achatinin(H) (ATNH), we have reported a non-invasive, blood based lymphoproliferation assay which measures the maximal lymphoproliferative dose (MLD) of ATN(H) to assess the status of 9-O-acetylated sialoglycoconjugates (9-OAcSGs) in patients with Acute lymphoblastic leukemia (ALL) (Mandal C, Sinha D, Sharma V, Bhattacharya DK. O-acetyl sialic acid binding lectin, as a probe for detection of subtle changes on the cell surface induced during acute lymphoblastic leukemia [ALL] and its clinical application. Ind J Biochem Biophys 1997;34:82; Sinha D, Mandal C, Bhattacharya DK. Development of a simple blood based lymphoproliferation assay to assess the clinical status of patients with acute lymphoblastic leukemia. Leuk Res 1999;13:309-312; Sinha D, Mandal C, Bhattacharya DK. A novel method for prognostic evaluation of childhood acute lymphoblastic leukemia. Leukemia 1999;13[in press]). Although the expression of 9-OAcSGs clearly serves as an index of treatment outcome, the assay has limitations in that it requires radioisotopes, i.e. [3H]-TdR. Therefore a colorimetric assay was developed as an alternative approach. The pre-treatment MLD, as measured by the colorimetric assay, was 0.15 +/- 0.02 microg which progressively increased during consolidation therapy (1.40 +/- 0.39 microg), maintenance therapy (4.20 +/- 1.60 microg) and in followed-up cases (5.20 +/- 0.43 microg) but sharply declined following relapse (0.25 +/- 0.02 microg). The colorimetric assay also showed a good correlation with radiometric assay (r = + 0.93) and their mean coefficient of inter-assay precision were also comparable (15.53% versus 14.86%). We therefore propose that the colorimetric assay is a safe, non-radiometric, user-friendly alternative for assessing individual chemotherapeutic responses in childhood ALL.

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Year:  1999        PMID: 10475619     DOI: 10.1016/s0145-2126(99)00093-4

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  6 in total

1.  O-acetylation of sialic acids is required for the survival of lymphoblasts in childhood acute lymphoblastic leukemia (ALL).

Authors:  Shyamasree Ghosh; Suman Bandyopadhyay; Kankana Mukherjee; Asish Mallick; Santanu Pal; Chhabinath Mandal; Dilip K Bhattacharya; Chitra Mandal
Journal:  Glycoconj J       Date:  2007-01       Impact factor: 2.916

2.  Specificity of the binding site of the sialic acid-binding lectin from ovine placenta, deduced from interactions with synthetic analogues.

Authors:  M F Troncoso; M M Iglesias; R Isecke; C W Todel; R Brossmer
Journal:  Glycoconj J       Date:  2000-10       Impact factor: 2.916

3.  9-O-acetylated sialic acids differentiating normal haematopoietic precursors from leukemic stem cells with high aldehyde dehydrogenase activity in children with acute lymphoblastic leukaemia.

Authors:  Suchandra Chowdhury; Sarmila Chandra; Chitra Mandal
Journal:  Glycoconj J       Date:  2014-10       Impact factor: 2.916

Review 4.  Functions and Biosynthesis of O-Acetylated Sialic Acids.

Authors:  Chitra Mandal; Reinhard Schwartz-Albiez; Reinhard Vlasak
Journal:  Top Curr Chem       Date:  2015

Review 5.  Post-Glycosylation Modification of Sialic Acid and Its Role in Virus Pathogenesis.

Authors:  Simon S Park
Journal:  Vaccines (Basel)       Date:  2019-11-01

6.  Flow-cytometric monitoring of disease-associated expression of 9-O-acetylated sialoglycoproteins in combination with known CD antigens, as an index for MRD in children with acute lymphoblastic leukaemia: a two-year longitudinal follow-up study.

Authors:  Suchandra Chowdhury; Suman Bandyopadhyay; Chandan Mandal; Sarmila Chandra; Chitra Mandal
Journal:  BMC Cancer       Date:  2008-02-01       Impact factor: 4.430

  6 in total

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