2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Progress in cancer neuroscience

      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

          Cancer of the central nervous system (CNS) can crosstalk systemically and locally in the tumor microenvironment and has become a topic of attention for tumor initiation and advancement. Recently studied neuronal and cancer interaction fundamentally altered the knowledge about glioma and metastases, indicating how cancers invade complex neuronal networks. This review systematically discussed the interactions between neurons and cancers and elucidates new therapeutic avenues. We have overviewed the current understanding of direct or indirect communications of neuronal cells with cancer and the mechanisms associated with cancer invasion. Besides, tumor‐associated neuronal dysfunction and the influence of cancer therapies on the CNS are highlighted. Furthermore, interactions between peripheral nervous system and various cancers have also been discussed separately. Intriguingly and importantly, it cannot be ignored that exosomes could mediate the “wireless communications” between nervous system and cancer. Finally, promising future strategies targeting neuronal–brain tumor interactions were reviewed. A great deal of work remains to be done to elucidate the neuroscience of cancer, and future more research should be directed toward clarifying the precise mechanisms of cancer neuroscience, which hold enormous promise to improve outcomes for a wide range of malignancies.

          Abstract

          Neurons and cancer cells’ synaptic communication can modulate cancer growth via neurotransmitters and voltage‐mediated mechanisms. Besides, paracrine signaling between cancer and nerve cells, for instance, the neuron‐mediated secretion of growth factors or neurotransmitters, modulates cancer growth in various tissues. The neuronal influence on malignant cells might be direct or affect other cells in TME. Cancer‐induced paracrine factors modulate nervous system to enhance neural activity in TME. Furthermore, cancers functionally control neural networks, and aberrant neural circuits stimulate tumor progression. Circulating factors released from cancer effects nervous system activity, whereas nervous system influences cancer growth by circulating molecules (hormones and progenitor cells) and alters immune system function.

          Related collections

          Most cited references202

          • Record: found
          • Abstract: found
          • Article: not found

          Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells.

          Exosomes are vesicles of endocytic origin released by many cells. These vesicles can mediate communication between cells, facilitating processes such as antigen presentation. Here, we show that exosomes from a mouse and a human mast cell line (MC/9 and HMC-1, respectively), as well as primary bone marrow-derived mouse mast cells, contain RNA. Microarray assessments revealed the presence of mRNA from approximately 1300 genes, many of which are not present in the cytoplasm of the donor cell. In vitro translation proved that the exosome mRNAs were functional. Quality control RNA analysis of total RNA derived from exosomes also revealed presence of small RNAs, including microRNAs. The RNA from mast cell exosomes is transferable to other mouse and human mast cells. After transfer of mouse exosomal RNA to human mast cells, new mouse proteins were found in the recipient cells, indicating that transferred exosomal mRNA can be translated after entering another cell. In summary, we show that exosomes contain both mRNA and microRNA, which can be delivered to another cell, and can be functional in this new location. We propose that this RNA is called "exosomal shuttle RNA" (esRNA).
            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

              Chimeric antigen receptor T-cell therapy — assessment and management of toxicities

              Chimeric antigen receptor (CAR)-T-cell therapies are showing great promise in the treatment of cancer, particularly B-cell malignancies, but are associated with characteristic, potentially fatal toxicities, principally cytokine-release syndrome, CAR-T-cell-related encephalopathy syndrome, and haemophagocytic lymphohistiocytosis/macrophage-activation syndrome. Herein, the CAR-T-cell-therapy-associated TOXicity (CARTOX) Working Group, comprising multidisciplinary investigators from various institutions with clinical experience in the use of a range of CAR-T-cell platforms, review these acute toxicities and provide monitoring, grading, and management recommendations.
                Bookmark

                Author and article information

                Contributors
                lanyulong@zju.edu.cn
                cq-chem@zju.edu.cn
                Neurosurgery@zju.edu.cn
                Journal
                MedComm (2020)
                MedComm (2020)
                10.1002/(ISSN)2688-2663
                MCO2
                MedComm
                John Wiley and Sons Inc. (Hoboken )
                2688-2663
                22 November 2023
                December 2023
                : 4
                : 6 ( doiID: 10.1002/mco2.v4.6 )
                : e431
                Affiliations
                [ 1 ] Department of Neurosurgery Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang China
                [ 2 ] Key Laboratory of Precise Treatment and Clinical Translational Research of Neurological Diseases Hangzhou Zhejiang China
                [ 3 ] Clinical Research Center for Neurological Diseases of Zhejiang Province Hangzhou China
                [ 4 ] Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, School of Pharmaceutical Science Zhejiang Chinese Medical University Hangzhou China
                [ 5 ] Department of Neurosurgery Beijing Tiantan Hospital, Capital Medical University Beijing China
                Author notes
                [*] [* ] Correspondence

                Yu‐Long Lan, Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310000, China.

                Email: lanyulong@ 123456zju.edu.cn

                Qi Chen, Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, School of Pharmaceutical Science, Zhejiang Chinese Medical University, Hangzhou 310053, China.

                Email: cq-chem@ 123456zju.edu.cn

                Yongjian Zhu, Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310000, China.

                Email: Neurosurgery@ 123456zju.edu.cn

                [#]

                Yu‐Long Lan and Shuang Zou contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-0995-4639
                https://orcid.org/0000-0002-5152-0079
                Article
                MCO2431
                10.1002/mco2.431
                10665600
                95892bf9-24ce-46cd-898b-dac31870ff1c
                © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 November 2023
                : 10 July 2023
                : 08 November 2023
                Page count
                Figures: 7, Tables: 0, Pages: 25, Words: 16193
                Funding
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: 82103480
                Funded by: Natural Science Foundation of Zhejiang Province , doi 10.13039/501100004731;
                Award ID: LQ22H090018
                Funded by: Research Project of Zhejiang Chinese Medical University
                Award ID: 2023JKZKTS25
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                December 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.5 mode:remove_FC converted:23.11.2023

                cancer,cancer neuroscience,interaction,neuron,neuroscience,treatment

                Comments

                Comment on this article