Author | Melzer, Michael Karl | dc.contributor.author |
Author | Arnold, Frank | dc.contributor.author |
Author | Stifter, Katja | dc.contributor.author |
Author | Zengerling, Friedemann | dc.contributor.author |
Author | Azoitei, Ninel | dc.contributor.author |
Author | Seufferlein, Thomas | dc.contributor.author |
Author | Bolenz, Christian | dc.contributor.author |
Author | Kleger, Alexander | dc.contributor.author |
Date of accession | 2023-03-20T11:12:32Z | dc.date.accessioned |
Available in OPARU since | 2023-03-20T11:12:32Z | dc.date.available |
Date of first publication | 2020-05-08 | dc.date.issued |
Abstract | Pancreatic ductal adenocarcinoma (PDAC) has still a dismal prognosis. Different factors such as mutational landscape, intra- and intertumoral heterogeneity, stroma, and immune cells impact carcinogenesis of PDAC associated with an immunosuppressive microenvironment. Different cell types with partly opposing roles contribute to this milieu. In recent years, immunotherapeutic approaches, including checkpoint inhibitors, were favored to treat cancers, albeit not every cancer entity exhibited benefits in a similar way. Indeed, immunotherapies rendered little success in pancreatic cancer. In this review, we describe the communication between the immune system and pancreatic cancer cells and propose some rationale why immunotherapies may fail in the context of pancreatic cancer. Moreover, we delineate putative strategies to sensitize PDAC towards immunological therapeutics and highlight the potential of targeting neoantigens. | dc.description.abstract |
Language | en | dc.language.iso |
Publisher | Universität Ulm | dc.publisher |
License | CC BY 4.0 International | dc.rights |
Link to license text | https://creativecommons.org/licenses/by/4.0/ | dc.rights.uri |
Keyword | PDAC | dc.subject |
Keyword | pancreatic cancer | dc.subject |
Keyword | immune checkpoints | dc.subject |
Keyword | immune microenvironment | dc.subject |
Dewey Decimal Group | DDC 610 / Medicine & health | dc.subject.ddc |
LCSH | Pancreas; Cancer | dc.subject.lcsh |
MeSH | Pancreatic neoplasms; Immunology | dc.subject.mesh |
MeSH | Immunotherapy | dc.subject.mesh |
Title | An immunological glance on pancreatic ductal adenocarcinoma | dc.title |
Resource type | Wissenschaftlicher Artikel | dc.type |
SWORD Date | 2022-09-05T17:15:20Z | dc.date.updated |
Version | publishedVersion | dc.description.version |
DOI | http://dx.doi.org/10.18725/OPARU-47805 | dc.identifier.doi |
URN | http://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-47881-5 | dc.identifier.urn |
GND | Bauchspeicheldrüsenkrebs | dc.subject.gnd |
GND | Immuntherapie | dc.subject.gnd |
Institution | UKU. Klinik für Innere Medizin I | uulm.affiliationSpecific |
Institution | UKU. Klinik für Urologie und Kinderurologie | uulm.affiliationSpecific |
Peer review | ja | uulm.peerReview |
DCMI Type | Text | uulm.typeDCMI |
Category | Publikationen | uulm.category |
DOI of original publication | 10.3390/ijms21093345 | dc.relation1.doi |
Source - Title of source | International Journal of Molecular Sciences | source.title |
Source - Place of publication | MDPI | source.publisher |
Source - Volume | 21 | source.volume |
Source - Issue | 9 | source.issue |
Source - Year | 2020 | source.year |
Source - Article number | 3345 | source.articleNumber |
Source - ISSN | 1661-6596 | source.identifier.issn |
Source - eISSN | 1422-0067 | source.identifier.eissn |
WoS | 000535581700316 | uulm.identifier.wos |
Bibliography | uulm | uulm.bibliographie |
DFG project uulm | Heisenberg / Zelluläre Plastizität im Pankreas - vom Krankheitsmodell über Gewebserneuerung zur personalisierten Medizin / DFG / 426789149 [KL 2544/1-1] | uulm.projectDFG |
DFG project uulm | Differenzierung von Pankreasgängen und -azini aus humanen pluripotenten Stammzellen zur Untersuchung des Pankreaskarzinoms / DFG / 426789343 [KL 2544/1-1] | uulm.projectDFG |
DFG project uulm | GRK 2254 / HEIST / Heterogenität und Evolution in soliden Tumoren (HEIST) / DFG / 288342734 [KL 2544/1-2] | uulm.projectDFG |
DFG project uulm | Screening nach und Validierung von neuen Kandidatengenen, die Pankreasentwicklung und Stammzellfitness regulieren / DFG /214644051 [KL 2544/7-1] | uulm.projectDFG |
DFG project uulm | Monogenetische Formen des juvenil sich manifestierenden Diabetes: neue Schritte in Richtung β-Zellentwicklung, -funktion und -überleben / DFG / 406674944 [KL 2544/5-1] | uulm.projectDFG |
Project uulm | BIU / Boehringer Ingelheim Ulm University BioCenter (BIU) / Forschungsverbund | uulm.projectOther |
Project uulm | Deutsche Krebshilfe / 111879 | uulm.projectOther |