7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Cellular collusion: cracking the code of immunosuppression and chemo resistance in PDAC

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Despite the efforts, pancreatic ductal adenocarcinoma (PDAC) is still highly lethal. Therapeutic challenges reside in late diagnosis and establishment of peculiar tumor microenvironment (TME) supporting tumor outgrowth. This stromal landscape is highly heterogeneous between patients and even in the same patient. The organization of functional sub-TME with different cellular compositions provides evolutive advantages and sustains therapeutic resistance. Tumor progressively establishes a TME that can suit its own needs, including proliferation, stemness and invasion. Cancer-associated fibroblasts and immune cells, the main non-neoplastic cellular TME components, follow soluble factors-mediated neoplastic instructions and synergize to promote chemoresistance and immune surveillance destruction. Unveiling heterotypic stromal-neoplastic interactions is thus pivotal to breaking this synergism and promoting the reprogramming of the TME toward an anti-tumor milieu, improving thus the efficacy of conventional and immune-based therapies. We underscore recent advances in the characterization of immune and fibroblast stromal components supporting or dampening pancreatic cancer progression, as well as novel multi-omic technologies improving the current knowledge of PDAC biology. Finally, we put into context how the clinic will translate the acquired knowledge to design new-generation clinical trials with the final aim of improving the outcome of PDAC patients.

          Related collections

          Most cited references214

          • Record: found
          • Abstract: found
          • Article: not found
          Is Open Access

          Cancer statistics, 2023

          Each year, the American Cancer Society estimates the numbers of new cancer cases and deaths in the United States and compiles the most recent data on population-based cancer occurrence and outcomes using incidence data collected by central cancer registries and mortality data collected by the National Center for Health Statistics. In 2023, 1,958,310 new cancer cases and 609,820 cancer deaths are projected to occur in the United States. Cancer incidence increased for prostate cancer by 3% annually from 2014 through 2019 after two decades of decline, translating to an additional 99,000 new cases; otherwise, however, incidence trends were more favorable in men compared to women. For example, lung cancer in women decreased at one half the pace of men (1.1% vs. 2.6% annually) from 2015 through 2019, and breast and uterine corpus cancers continued to increase, as did liver cancer and melanoma, both of which stabilized in men aged 50 years and older and declined in younger men. However, a 65% drop in cervical cancer incidence during 2012 through 2019 among women in their early 20s, the first cohort to receive the human papillomavirus vaccine, foreshadows steep reductions in the burden of human papillomavirus-associated cancers, the majority of which occur in women. Despite the pandemic, and in contrast with other leading causes of death, the cancer death rate continued to decline from 2019 to 2020 (by 1.5%), contributing to a 33% overall reduction since 1991 and an estimated 3.8 million deaths averted. This progress increasingly reflects advances in treatment, which are particularly evident in the rapid declines in mortality (approximately 2% annually during 2016 through 2020) for leukemia, melanoma, and kidney cancer, despite stable/increasing incidence, and accelerated declines for lung cancer. In summary, although cancer mortality rates continue to decline, future progress may be attenuated by rising incidence for breast, prostate, and uterine corpus cancers, which also happen to have the largest racial disparities in mortality.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Hallmarks of Cancer: New Dimensions

            The hallmarks of cancer conceptualization is a heuristic tool for distilling the vast complexity of cancer phenotypes and genotypes into a provisional set of underlying principles. As knowledge of cancer mechanisms has progressed, other facets of the disease have emerged as potential refinements. Herein, the prospect is raised that phenotypic plasticity and disrupted differentiation is a discrete hallmark capability, and that nonmutational epigenetic reprogramming and polymorphic microbiomes both constitute distinctive enabling characteristics that facilitate the acquisition of hallmark capabilities. Additionally, senescent cells, of varying origins, may be added to the roster of functionally important cell types in the tumor microenvironment. SIGNIFICANCE: Cancer is daunting in the breadth and scope of its diversity, spanning genetics, cell and tissue biology, pathology, and response to therapy. Ever more powerful experimental and computational tools and technologies are providing an avalanche of "big data" about the myriad manifestations of the diseases that cancer encompasses. The integrative concept embodied in the hallmarks of cancer is helping to distill this complexity into an increasingly logical science, and the provisional new dimensions presented in this perspective may add value to that endeavor, to more fully understand mechanisms of cancer development and malignant progression, and apply that knowledge to cancer medicine.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy.

              Cancer immunotherapy can induce long lasting responses in patients with metastatic cancers of a wide range of histologies. Broadening the clinical applicability of these treatments requires an improved understanding of the mechanisms limiting cancer immunotherapy. The interactions between the immune system and cancer cells are continuous, dynamic, and evolving from the initial establishment of a cancer cell to the development of metastatic disease, which is dependent on immune evasion. As the molecular mechanisms of resistance to immunotherapy are elucidated, actionable strategies to prevent or treat them may be derived to improve clinical outcomes for patients.
                Bookmark

                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/1942185Role: Role:
                URI : https://loop.frontiersin.org/people/870563Role: Role:
                Role: Role:
                URI : https://loop.frontiersin.org/people/2581727Role: Role:
                URI : https://loop.frontiersin.org/people/2581653Role: Role:
                URI : https://loop.frontiersin.org/people/1040163Role: Role:
                Role: Role:
                URI : https://loop.frontiersin.org/people/674955Role: Role:
                URI : https://loop.frontiersin.org/people/138311Role: Role:
                URI : https://loop.frontiersin.org/people/126593Role: Role: Role:
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                16 May 2024
                2024
                : 15
                : 1341079
                Affiliations
                [1] 1 Department of Medicine, University of Verona , Verona, Italy
                [2] 2 Department of Engineering for Innovation Medicine, University of Verona , Verona, Italy
                [3] 3 Medical Oncology, Department of Translational Medicine, Catholic University of the Sacred Heart , Rome, Italy
                [4] 4 Medical Oncology, Department of Medical and Surgical Sciences, Fondazione Policlinico Universitario Agostino Gemelli Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS) , Rome, Italy
                [5] 5 General and Pancreatic Surgery Unit, Pancreas Institute, University of Verona , Verona, Italy
                [6] 6 ARC-Net Research Centre, University of Verona , Verona, Italy
                Author notes

                Edited by: Louis M. Weiner, Georgetown University, United States

                Reviewed by: Willem de Koning, Erasmus Medical Center, Netherlands

                Nune Markosyan, University of Pennsylvania, United States

                Elisa Espinet, University of Barcelona, Spain

                *Correspondence: Francesco De Sanctis, francesco.desanctis@ 123456univr.it ; Stefano Ugel, Stefano.ugel@ 123456univr.it

                †These authors share first authorship

                ‡These authors share last authorship

                Article
                10.3389/fimmu.2024.1341079
                11137177
                38817612
                d62f480c-67e5-4835-9a81-266e2f2fa7b8
                Copyright © 2024 Musiu, Lupo, Agostini, Lionetto, Bevere, Paiella, Carbone, Corbo, Ugel and De Sanctis

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 19 November 2023
                : 02 May 2024
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 215, Pages: 20, Words: 9051
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was jointly supported by PRIN programs of the Italian Ministry of Education, University, and Research (MIUR, PI: De Sanctis F., CUP: B39J22001200001); AIRC (PI: Carbone C Grant No. 23681; PI: Corbo V. Grant No. 18178, PI: Ugel S. Grant No. 21509 and 28730); EU (MSCA project PRECODE, PI: Corbo V. Grant No 861196); PNRR programs of the Italian MUR (Project “National Center for Gene Therapy and Drugs based on RNA Technology”, application code CN00000041, Mission 4, Component 2 Investment 1.4, funded from the European Union - NextGenerationEU, MUR Directorial Decree No. 1035 of 17 June 2022, CUP B33C22000630001; PI: Ugel S). CM was supported by an AIRC fellowship for Italy (Call 2022), and was supported by Fondazione Umberto Veronesi (Call 2023). MB was supported by AIRC fellowships for Italy (28054; 29829).
                Categories
                Immunology
                Review
                Custom metadata
                Cancer Immunity and Immunotherapy

                Immunology
                pdac - pancreatic ductal adenocarcinoma,immunotherapy,tme (tumor microenvironment),cancer associated fibroblast (caf),mdsc (myeloid-derived suppressor cells),tils (tumor infiltrating lymphocytes),immunosuppression

                Comments

                Comment on this article

                scite_
                0
                0
                0
                0
                Smart Citations
                0
                0
                0
                0
                Citing PublicationsSupportingMentioningContrasting
                View Citations

                See how this article has been cited at scite.ai

                scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

                Similar content109

                Cited by3

                Most referenced authors4,982