L1TD1 - a prognostic marker for colon cancer.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
23 Jul 2019
Historique:
received: 19 12 2018
accepted: 18 07 2019
entrez: 25 7 2019
pubmed: 25 7 2019
medline: 15 2 2020
Statut: epublish

Résumé

Prognostic markers specific to a particular cancer type can assist in the evaluation of survival probability of patients and help clinicians to assess the available treatment modalities. Gene expression data was analyzed from three independent colon cancer microarray gene expression data sets (N = 1052). Survival analysis was performed for the three data sets, stratified by the expression level of the LINE-1 type transposase domain containing 1 (L1TD1). Correlation analysis was performed to investigate the role of the interactome of L1TD1 in colon cancer patients. We found L1TD1 as a novel positive prognostic marker for colon cancer. Increased expression of L1TD1 associated with longer disease-free survival in all the three data sets. Our results were in contrast to a previous study on medulloblastoma, where high expression of L1TD1 was linked with poor prognosis. Notably, in medulloblastoma L1TD1 was co-expressed with its interaction partners, whereas our analysis revealed lack of co-expression of L1TD1 with its interaction partners in colon cancer. Our results identify increased expression of L1TD1 as a prognostic marker predicting longer disease-free survival in colon cancer patients.

Sections du résumé

BACKGROUND BACKGROUND
Prognostic markers specific to a particular cancer type can assist in the evaluation of survival probability of patients and help clinicians to assess the available treatment modalities.
METHODS METHODS
Gene expression data was analyzed from three independent colon cancer microarray gene expression data sets (N = 1052). Survival analysis was performed for the three data sets, stratified by the expression level of the LINE-1 type transposase domain containing 1 (L1TD1). Correlation analysis was performed to investigate the role of the interactome of L1TD1 in colon cancer patients.
RESULTS RESULTS
We found L1TD1 as a novel positive prognostic marker for colon cancer. Increased expression of L1TD1 associated with longer disease-free survival in all the three data sets. Our results were in contrast to a previous study on medulloblastoma, where high expression of L1TD1 was linked with poor prognosis. Notably, in medulloblastoma L1TD1 was co-expressed with its interaction partners, whereas our analysis revealed lack of co-expression of L1TD1 with its interaction partners in colon cancer.
CONCLUSIONS CONCLUSIONS
Our results identify increased expression of L1TD1 as a prognostic marker predicting longer disease-free survival in colon cancer patients.

Identifiants

pubmed: 31337362
doi: 10.1186/s12885-019-5952-2
pii: 10.1186/s12885-019-5952-2
pmc: PMC6651905
doi:

Substances chimiques

Biomarkers, Tumor 0
L1TD1 protein, human 0
Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

727

Subventions

Organisme : Academy of Finland
ID : 265723
Organisme : Academy of Finland
ID : 250114, 292335, 294337, 292482, and 31444
Organisme : Academy of Finland
ID : 296801, 304995, 310561 and 313343
Organisme : European Research Council
ID : 677943
Pays : International
Organisme : H2020 European Research Council
ID : 675395
Organisme : Juvenile Diabetes Research Foundation International
ID : 2-2013-32

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Auteurs

Deepankar Chakroborty (D)

Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Institute of Biomedicine, Faculty of Medicine, University of Turku, Turku, Finland.

Maheswara Reddy Emani (MR)

Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.

Riku Klén (R)

Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.

Camilla Böckelman (C)

Research Programs Unit, Translational Cancer Biology, University of Helsinki, Helsinki, Finland.
Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Jaana Hagström (J)

Research Programs Unit, Translational Cancer Biology, University of Helsinki, Helsinki, Finland.
Department of Pathology and Oral Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Caj Haglund (C)

Research Programs Unit, Translational Cancer Biology, University of Helsinki, Helsinki, Finland.
Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Ari Ristimäki (A)

Department of Pathology, HUSLAB, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Genome-Scale Biology Research program, University of Helsinki, 00290, Helsinki, Finland.

Riitta Lahesmaa (R)

Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland. riitta.lahesmaa@utu.fi.

Laura L Elo (LL)

Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland. laura.elo@utu.fi.

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Classifications MeSH