Evidence map›Paper›PMID 26681737›Full record

ArticleGut2017

T cell neoepitope discovery in colorectal cancer by high throughput profiling of somatic mutations in expressed genes.

Daniele Mennonna, Cristina Maccalli, Michele C Romano, Claudio Garavaglia, Filippo Capocefalo, Roberta Bordoni, Marco Severgnini, Gianluca De Bellis, John Sidney, Alessandro Sette and 15 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04622423 (Advanced Immune Gene and Cell Therapies for Liver Metastases), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04622423 recruitingnot on this mapstarted 2019, after this paper: background citation

Advanced Immune Gene and Cell Therapies for Liver Metastases

TypeobservationalSponsorIRCCS San RaffaeleRan2019 to 2030Enrolled625ConditionsPancreatic Ductal Adenocarcinoma (PDAC), Colorectal Cancer (CRC), Liver Metastasis, IPMN, Pancreatic
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
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  3. New insights on anti-tumor immunity of CD8Journal of translational medicine · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 7 institutions in 3 countries.

Daniele MennonnaDivision of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
Cristina MaccalliDivision of Experimental Oncology, San Raffaele Scientific Institute, Milan, Italy.
Michele C RomanoDivision of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
Claudio GaravagliaDivision of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
Filippo CapocefaloDivision of Experimental Oncology, San Raffaele Scientific Institute, Milan, Italy.
Roberta BordoniInstitute for Biomedical Technologies, National Research Council, Segrate, Italy.
Marco SevergniniInstitute for Biomedical Technologies, National Research Council, Segrate, Italy.
Gianluca De BellisInstitute for Biomedical Technologies, National Research Council, Segrate, Italy.
John SidneyLa Jolla Institute for Allergy & Immunology, La Jolla, California, USA.
Alessandro SetteLa Jolla Institute for Allergy & Immunology, La Jolla, California, USA.
Alessandro GoriInstitute of Molecular Recognition Chemistry, National Research Council, Milan, Italy.
Renato LonghiInstitute of Molecular Recognition Chemistry, National Research Council, Milan, Italy.
Marco BragaDepartment of Surgery, San Raffaele Scientific Institute, Milan, Italy.
Luca GhirardelliDepartment of Surgery, San Raffaele Scientific Institute, Milan, Italy.
Ludovica BaldariDepartment of Surgery, San Raffaele Scientific Institute, Milan, Italy.
Elena OrsenigoDepartment of Surgery, San Raffaele Scientific Institute, Milan, Italy.
Luca AlbarelloDepartment of Pathology, San Raffaele Scientific Institute, Milano, Italy.
Elisabetta ZinoUnit of Molecular and Functional Immunogenetics, San Raffaele Scientific Institute, Milan, Italy.
Katharina FleischhauerUnit of Molecular and Functional Immunogenetics, San Raffaele Scientific Institute, Milan, Italy.
Gina MazzolaDepartment of Medical Sciences, Center for Transplantation Biology and Immunogenetics, University of Turin, Turin, Italy.
Norma FerreroDepartment of Medical Sciences, Center for Transplantation Biology and Immunogenetics, University of Turin, Turin, Italy.
Antonio AmorosoDepartment of Medical Sciences, Center for Transplantation Biology and Immunogenetics, University of Turin, Turin, Italy.
Giulia CasoratiDivision of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
Giorgio ParmianiDivision of Experimental Oncology, San Raffaele Scientific Institute, Milan, Italy.
Paolo DellabonaDivision of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
San Raffaele University of Rome · ITVita-Salute San Raffaele University · ITUniversity of Turin · ITInstitute of Chemistry of Molecular Recognition · ITLa Jolla Institute for Immunology · USNational Research Council · ITInstitute of Biomedical Technologies · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePatient-specific (unique) tumour antigens, encoded by somatically mutated cancer genes, generate neoepitopes that are implicated in the induction of tumour-controlling T cell responses. Recent advancements in massive DNA sequencing combined with robust T cell epitope predictions have allowed their systematic identification in several malignancies.

designWe undertook the identification of unique neoepitopes in colorectal cancers (CRCs) by using high-throughput sequencing of cDNAs expressed by standard cancer cell cultures, and by related cancer stem/initiating cells (CSCs) cultures, coupled with a reverse immunology approach not requiring human leukocyte antigen (HLA) allele-specific epitope predictions.

resultsSeveral unique mutated antigens of CRC, shared by standard cancer and related CSC cultures, were identified by this strategy. CD8

conclusionsThese results provide a proof-of-concept approach for the identification of unique neoepitopes that are immunogenic in patients with CRC and can also target T cells against the most aggressive CSC component.

Indexed as

Adenomatous Polyposis Coli ProteinCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Cycle ProteinsClass I Phosphatidylinositol 3-KinasesColorectal NeoplasmsDNA, ComplementaryDNA Mutational AnalysisEpitopes, T-LymphocyteF-Box ProteinsF-Box-WD Repeat-Containing Protein 7Gene ExpressionHigh-Throughput Screening AssaysHLA AntigensHumansNeoplastic Stem CellsAdenomatous Polyposis Coli ProteinAPC protein, humanCell Cycle ProteinsClass I Phosphatidylinositol 3-KinasesDNA, ComplementaryEpitopes, T-LymphocyteF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanHLA AntigensKRAS protein, humanPhosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene Proteins p21(ras)Smad4 ProteinSMAD4 protein, humanTumor Suppressor Protein p53Ubiquitin-Protein LigasesANTIGENSCANCER IMMUNOBIOLOGYCOLORECTAL CANCERGENE MUTATIONIMMUNE RESPONSE

Identifiers

PMID26681737
PMCPMC5534766
OpenAlexW2196549479

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.