Carbohydrate antigens Lewis a and Lewis b act as tumor markers cooperating with CA19.9 in the management of PDAC patients.

Carbohydrate antigen ELISA Glycosylation Histo-blood group antigens Mucin Pancreas cancer Tumor marker

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
03 Oct 2024
Historique:
received: 13 08 2024
revised: 24 09 2024
accepted: 03 10 2024
medline: 6 10 2024
pubmed: 6 10 2024
entrez: 5 10 2024
Statut: aheadofprint

Résumé

CA19.9 is the unique marker recommended for the preoperative staging and the follow-up of patients suffering from pancreatic ductal adenocarcinoma (PDAC) but up to 30% of PDAC patients maintain normal CA19.9 values and cannot be monitored in this way. Lewis a (Lea Galβ1,3[Fucα1,4]GlcNAc) and b (Leb, Fucα1,2Galβ1,3[Fucα1,4]GlcNAc) are antigens which are structurally similar to sialyl-Lewis a (Siaα2,3Galβ1,3[Fucα1,4]GlcNAc), the epitope of CA19.9. We set an ELISA procedure determining the levels of Lea, Leb, and CA19.9 in the blood of healthy individuals or PDAC patients. Moreover, such antigens were also detected in cancer resections by immunofluorescence microscopy, and the levels of glycosyltransferase transcripts involved in Lewis antigen biosynthesis were determined by RT-qPCR. In our cohort of 116 healthy individuals, the distribution of circulating Lea and Leb was similar to that of CA19.9, allowing us to set putative cutoff values for both antigens. In a cohort of 115 PDAC patients, the differential distribution with respect to the controls was statistically significant for both antigens (p < 0.001). Out of 37 patients presenting normal CA19.9 values, 15 patients presented Lea or Leb above the cutoffs. By immunofluorescence, Lea, Leb and CA19.9 were all detected in cancer resections and expression levels were heterogeneous among patients in terms of intensity, localization and diffusion. The levels of relevant glycosyltransferase transcripts were found to be heterogeneous between cancers of different patients and no association was detectable with the levels of any circulating antigen. The concurrent quantification of Lea and Leb together with CA19.9 improves the management of PDAC patients.

Sections du résumé

BACKGROUND BACKGROUND
CA19.9 is the unique marker recommended for the preoperative staging and the follow-up of patients suffering from pancreatic ductal adenocarcinoma (PDAC) but up to 30% of PDAC patients maintain normal CA19.9 values and cannot be monitored in this way. Lewis a (Lea Galβ1,3[Fucα1,4]GlcNAc) and b (Leb, Fucα1,2Galβ1,3[Fucα1,4]GlcNAc) are antigens which are structurally similar to sialyl-Lewis a (Siaα2,3Galβ1,3[Fucα1,4]GlcNAc), the epitope of CA19.9.
METHODS METHODS
We set an ELISA procedure determining the levels of Lea, Leb, and CA19.9 in the blood of healthy individuals or PDAC patients. Moreover, such antigens were also detected in cancer resections by immunofluorescence microscopy, and the levels of glycosyltransferase transcripts involved in Lewis antigen biosynthesis were determined by RT-qPCR.
RESULTS RESULTS
In our cohort of 116 healthy individuals, the distribution of circulating Lea and Leb was similar to that of CA19.9, allowing us to set putative cutoff values for both antigens. In a cohort of 115 PDAC patients, the differential distribution with respect to the controls was statistically significant for both antigens (p < 0.001). Out of 37 patients presenting normal CA19.9 values, 15 patients presented Lea or Leb above the cutoffs. By immunofluorescence, Lea, Leb and CA19.9 were all detected in cancer resections and expression levels were heterogeneous among patients in terms of intensity, localization and diffusion. The levels of relevant glycosyltransferase transcripts were found to be heterogeneous between cancers of different patients and no association was detectable with the levels of any circulating antigen.
CONCLUSIONS CONCLUSIONS
The concurrent quantification of Lea and Leb together with CA19.9 improves the management of PDAC patients.

Identifiants

pubmed: 39368686
pii: S0009-8981(24)02243-5
doi: 10.1016/j.cca.2024.119990
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

119990

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Rossella Indellicato (R)

Dipartimento di Scienze della Salute, University of Milan, Milano, Italy.

Michele Dei Cas (M)

Dipartimento di Scienze della Salute, University of Milan, Milano, Italy.

Aida Zulueta (A)

Istituti Clinici Scientifici Maugeri IRCCS, Department of Neurorehabilitation of the Milan Institute, Milano, Italy.

Anna Caretti (A)

Dipartimento di Scienze della Salute, University of Milan, Milano, Italy.

Delfina Tosi (D)

Dipartimento di Scienze della Salute, University of Milan, Milano, Italy; Unità Operativa di Anatomia Patologia, San Paolo Hospital, Milano, Italy.

Claudia Cigala (C)

Unità Operativa di Anatomia Patologia, San Paolo Hospital, Milano, Italy.

Gaetano Bulfamante (G)

Dipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche, University of Milan, Milano, Italy.

Enrico De Nicola (E)

Unità Operativa Chirurgia II, San Paolo Hospital, Milano, Italy.

Giovanna Scifo (G)

Unità Operativa Chirurgia II, San Paolo Hospital, Milano, Italy.

Enrico Opocher (E)

Dipartimento di Scienze della Salute, University of Milan, Milano, Italy; Unità Operativa Chirurgia II, San Paolo Hospital, Milano, Italy.

Daniela Pistillo (D)

Biology Resource Center - Humanitas Research Hospital, Rozzano, MI, Italy.

Gennaro Nappo (G)

Pancreatic Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.

Alessandro Zerbi (A)

Pancreatic Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.

Marco Trinchera (M)

Dipartimento di Medicina e Chirurgia, University of Insubria, Varese, Italy. Electronic address: marco.trinchera@uninsubria.it.

Classifications MeSH