Evidence map›Paper›PMID 17784873›Full record

ArticleCancer science2007

Identification of human leukocyte antigen-A24-restricted epitope peptides derived from gene products upregulated in lung and esophageal cancers as novel targets for immunotherapy.

Takako Suda, Takuya Tsunoda, Yataro Daigo, Yusuke Nakamura, Hideaki Tahara

12 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Cancer science, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 12 registered trials, which are not on this map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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.

NCT00561275 phase1completednot on this map

Phase 1 Study of Multiple Peptide Vaccine Therapy and GM-CSF in Treating Patients With Esophageal Cancer

TypeinterventionalSponsorJapanese Foundation for Cancer ResearchRan2007 to 2008Enrolled6ConditionsEsophageal CancerArmsLY6K, VEGFR1, VEGFR2
NCT00624182 phase1suspendednot on this mapstarted 2008, after this paper: background citation

Phase 1 Study of Gemcitabine With Vaccine Therapy Targeting Tumor Antigen, URLC10, For The Patients With Unresectable or Recurrent Bile Duct Cancer

TypeinterventionalSponsorAkita University HospitalRan2008 to 2016Enrolled9ConditionsBile Duct CancerArmsPeptide vaccine for URLC10, Gemcitabine
NCT00673777 phase1 / phase2unknown statusnot on this mapstarted 2008, after this paper: background citation

Phase I/II Study of Multiple-Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*0201 in Treating Patients With Refractory Non-Small Cell Lung Cancer

TypeinterventionalSponsorTokyo UniversityRan2008 to 2009Enrolled14ConditionsNon Small Cell Lung CancerArmsURLC10, VEGFR1 and VEGFR2
NCT00674258 phase1 / phase2unknown statusnot on this mapstarted 2008, after this paper: background citation

Phase I/II Study of Multiple-Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*0201 in Treating Patients With Refractory Non-Small Cell Lung Cancer

TypeinterventionalSponsorTokyo UniversityRan2008 to 2009Enrolled14ConditionsNon Small Cell Lung CancerArmsURLC10, TTK and KOC1
NCT00682227 phase1unknown statusnot on this map

Phase I Study of Peptide Vaccination Therapy Using Novel Cancer Testis Antigens for Locally Advanced, Recurrent, or Metastatic Esophageal Squamous Cell Carcinoma

TypeinterventionalSponsorUniversity of YamanashiRan2006 to 2009Enrolled10ConditionsEsophageal CancerArmsTTK, LY6K, and IMP-3 peptides
NCT01069575 phase1completednot on this mapstarted 2010, after this paper: background citation

Phase I Study of Cancer Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*24 (URLC10,CDCA1,KIF20A) in Patients With Non-small Cell Lung Cancer Refractory to Standard Therapy

TypeinterventionalSponsorShiga UniversityRan2010 to 2019Enrolled18ConditionsNon-Small Cell Lung CancerArmsHLA-A*2402restricted URLC10, CDCA1, and KIF20A peptides
NCT01069640 phase1completednot on this mapstarted 2010, after this paper: background citation

Phase I Study of Cancer Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*02 (URLC10) in Patients With Non-small Cell Lung Cancer Refractory to Standard Therapy

TypeinterventionalSponsorShiga UniversityRan2010 to 2019Enrolled9ConditionsNon-small Cell Lung CancerArmsHLA-A*0201 or HLA-A*0206-restricted URLC10 peptides
NCT01069653 phase1completednot on this mapstarted 2010, after this paper: background citation

Phase I Study of Cancer Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*24 (CDCA1,KIF20A) in Patients With Small Cell Lung Cancer Refractory to Standard Therapy

TypeinterventionalSponsorShiga UniversityRan2010 to 2019Enrolled9ConditionsSmall Cell Lung CancerArmsHLA-A*2402-restricted CDCA1 and KIF20A peptides
NCT01592617 phase2unknown statusnot on this mapstarted 2012, after this paper: background citation

Phase II Study of Peptide Cancer Vaccine S-488410 to Treat Advanced Non-Small Cell Lung Cancer

TypeinterventionalSponsorShiga UniversityRan2012 to 2015Enrolled45ConditionsCarcinoma, Non-Small-Cell LungArmsS-488410
NCT01949701 phase1 / phase2completednot on this mapstarted 2011, after this paper: background citation

Phase I/II Study Using Epitope Peptide Restricted to HLA-A*24 (URLC10) in Patients With Disease Controlled Advanced Non-small Cell Lung Cancer

TypeinterventionalSponsorShiga UniversityRan2011 to 2019Enrolled6ConditionsNon-small Cell Lung CancerArmsHLA-A*0201restricted URLC10 peptides with adjuvant
NCT01950156 phase1 / phase2completednot on this mapstarted 2011, after this paper: background citation

Phase I/II Study Using Epitope Peptide Restricted to HLA-A*24 (URLC10,CDCA1,KIF20A) in Patients With Disease Controlled Advanced Non-small Cell Lung Cancer

TypeinterventionalSponsorShiga UniversityRan2011 to 2019Enrolled6ConditionsNon-small Cell Lung CancerArmsHLA-A*2402restricted URLC10, CDCA1, and KIF20A peptides with adjuvant
NCT02410369 phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

Phase II Study of S-588410 as Maintenance Monotherapy After Adjuvant Chemotherapy in Patients With Completely Resected Non-small- Cell Lung Cancer

TypeinterventionalSponsorTokyo UniversityRan2015 to 2021Enrolled60ConditionsNon-small- Cell Lung CancerArmsS-588410, Placebo
3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 120 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Silencing LY6K Suppresses CD44Current issues in molecular biology · 2024
    Article
  9. IGF2BPs as novel mGenes & diseases · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. The immune landscape of esophageal cancer.Cancer communications (London, England) · 2019
    Review
  18. Article
  19. Review
  20. Article

1 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Takako Suda1Department of Surgery and Bioengineering, Advanced Clinical Research Center, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Takuya Tsunoda
Yataro Daigo
Yusuke Nakamura
Hideaki Tahara
The University of Tokyo · JPBioengineering Center · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For the development of cancer vaccine therapies, we have searched for possible epitope peptides that can elicit cytotoxic T lymphocytes (CTL) to the TTK protein kinase (TTK), lymphocyte antigen 6 complex locus K (LY6K) and insulin-like growth factor (IGF)-II mRNA binding protein 3 (IMP-3), which were previously identified to be transactivated in the majority of lung and esophageal cancers. We screened 31, 17 and 17 candidate human leukocyte antigen (HLA)-A*2402-binding peptides to parts of TTK, LY6K and IMP-3, respectively. As a result, we successfully established strong CTL clones stimulated by TTK-567 (SYRNEIAYL), LY6K-177 (RYCNLEGPPI) and IMP-3-508 (KTVNELQNL) that have specific cytotoxic activities against the HLA-A24-positive target cells pulsed with the candidate peptides. Subsequent analysis of the CTL clones also revealed their cytotoxic activities against lung and esophageal tumor cells that endogenously express TTK, LY6K or IMP-3. A cold target inhibition assay further confirmed that the CTL cell clones specifically recognized the MHC class I–peptide complex. Our results strongly imply that TTK, LY6K and IMP-3 are novel tumor-associated antigens recognized by CTL, and TTK-567 (SYRNEIAYL), LY6K-177 (RYCNLEGPPI) and IMP-3-508 (KTVNELQNL) are HLA-A24-restricted epitope peptides that can induce potent and specific immune responses against lung and esophageal cancer cells expressing TTK, LY6K and IMP-3.

Indexed as

Amino Acid SequenceAntigens, LyAntigens, NeoplasmBiomarkers, TumorCancer VaccinesCell Cycle ProteinsCell LineCell Line, TumorCells, CulturedCytotoxicity, ImmunologicCytotoxicity Tests, ImmunologicEpitopes, T-LymphocyteEsophageal NeoplasmsGPI-Linked ProteinsHLA-A24 AntigenHumansAntigens, LyAntigens, NeoplasmBiomarkers, TumorCancer VaccinesCell Cycle ProteinsEpitopes, T-LymphocyteGPI-Linked ProteinsHLA-A*24:02 antigenHLA-A24 AntigenIGF2BP3 protein, humanLY6K protein, humanPeptidesProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRNA-Binding ProteinsTTK protein, human

Identifiers

PMID17784873
PMCPMC11159329
OpenAlexW1990143240

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 6 more above

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.