Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker

Abstract Objective The discovery and characterization of tumor associated antigens is increasingly important to advance the field of immuno-oncology. In this regard, labyrinthin has been implicated as a neoantigen found on the cell surface of adenocarcinomas. Data on the (1) topology, (2) amino acid...

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Main Authors: Ankit Sharma, Michael Babich, Tianhong Li, James A. Radosevich
Format: Article
Language:English
Published: BMC 2023-07-01
Series:BMC Research Notes
Subjects:
Online Access:https://doi.org/10.1186/s13104-023-06373-4
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author Ankit Sharma
Michael Babich
Tianhong Li
James A. Radosevich
author_facet Ankit Sharma
Michael Babich
Tianhong Li
James A. Radosevich
author_sort Ankit Sharma
collection DOAJ
description Abstract Objective The discovery and characterization of tumor associated antigens is increasingly important to advance the field of immuno-oncology. In this regard, labyrinthin has been implicated as a neoantigen found on the cell surface of adenocarcinomas. Data on the (1) topology, (2) amino acid (a.a.) homology analyses and (3) cell surface localization of labyrinthin by fluorescent activated cell sorter (FACS) are studied in support of labyrinthin as a novel, pan-adenocarcinoma marker. Results Bioinformatics analyses predict labyrinthin as a type II protein with calcium binding domain(s), N-myristoylation sites, and kinase II phosphorylation sites. Sequence homologies for labyrinthin (255 a.a.) were found vs. the intracellular aspartyl/asparaginyl beta-hydroxylase (ASPH; 758 a.a.) and the ASPH-gene related protein junctate (299 a.a.), which are both type II proteins. Labyrinthin was detected by FACS on only non-permeablized A549 human lung adenocarcinoma cells, but not on normal WI-38 human lung fibroblasts nor primary cultures of normal human glandular-related cells. Microscopic images of immunofluorescent labelled MCA 44-3A6 binding to A549 cells at random cell cycle stages complement the FACS results by further showing that labyrinthin persisted on the cell surfaces along with some cell internalization for greater than 20 min.
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spelling doaj.art-7a5e6d2c90f04a4b9ccd7548bb9111852023-07-09T11:05:13ZengBMCBMC Research Notes1756-05002023-07-011611610.1186/s13104-023-06373-4Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarkerAnkit Sharma0Michael Babich1Tianhong Li2James A. Radosevich3LabyRx Immunologic Therapeutics LimitedLabyRx Immunologic Therapeutics LimitedDivision of Hematology & Oncology, University of California Davis Comprehensive Cancer CenterLabyRx Immunologic Therapeutics LimitedAbstract Objective The discovery and characterization of tumor associated antigens is increasingly important to advance the field of immuno-oncology. In this regard, labyrinthin has been implicated as a neoantigen found on the cell surface of adenocarcinomas. Data on the (1) topology, (2) amino acid (a.a.) homology analyses and (3) cell surface localization of labyrinthin by fluorescent activated cell sorter (FACS) are studied in support of labyrinthin as a novel, pan-adenocarcinoma marker. Results Bioinformatics analyses predict labyrinthin as a type II protein with calcium binding domain(s), N-myristoylation sites, and kinase II phosphorylation sites. Sequence homologies for labyrinthin (255 a.a.) were found vs. the intracellular aspartyl/asparaginyl beta-hydroxylase (ASPH; 758 a.a.) and the ASPH-gene related protein junctate (299 a.a.), which are both type II proteins. Labyrinthin was detected by FACS on only non-permeablized A549 human lung adenocarcinoma cells, but not on normal WI-38 human lung fibroblasts nor primary cultures of normal human glandular-related cells. Microscopic images of immunofluorescent labelled MCA 44-3A6 binding to A549 cells at random cell cycle stages complement the FACS results by further showing that labyrinthin persisted on the cell surfaces along with some cell internalization for greater than 20 min.https://doi.org/10.1186/s13104-023-06373-4Pan-tumor targetBiomarkerNeo-antigenAdenocarcinomaTumor associated antigenTumor specific antigen
spellingShingle Ankit Sharma
Michael Babich
Tianhong Li
James A. Radosevich
Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
BMC Research Notes
Pan-tumor target
Biomarker
Neo-antigen
Adenocarcinoma
Tumor associated antigen
Tumor specific antigen
title Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
title_full Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
title_fullStr Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
title_full_unstemmed Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
title_short Topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
title_sort topology and adenocarcinoma cell localization dataset on the labyrinthin diapeutic biomarker
topic Pan-tumor target
Biomarker
Neo-antigen
Adenocarcinoma
Tumor associated antigen
Tumor specific antigen
url https://doi.org/10.1186/s13104-023-06373-4
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AT tianhongli topologyandadenocarcinomacelllocalizationdatasetonthelabyrinthindiapeuticbiomarker
AT jamesaradosevich topologyandadenocarcinomacelllocalizationdatasetonthelabyrinthindiapeuticbiomarker