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      Cancer Immunology with a Focus on Understudied Cancers as Targets for Immunotherapy

      editorial
      1 , 2
      International Journal of Molecular Sciences
      MDPI

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          Abstract

          A number of immune therapeutic approaches have been transitioning from being experimental to being incorporated as standard approaches, either alone or in conjunction with other therapies. However, this has not been uniformly implemented or even tested across all cancer types. For example, immune therapies ranging from checkpoint inhibitory antibodies, cytokine therapies and tumor vaccines have been extensively tested and used as a treatment for melanoma. Immunotherapy for lung cancers has also received considerable attention. While immunotherapeutic approaches to treatment of leukemia have become quite common, this is been more sporadic in solid tumors. Since immunotherapy has not been uniformly implemented or even tested across solid cancer types, this Editorial and the articles in this special issue focused on immunotherapy for solid cancers and, in particular, solid cancers that have been understudied as targets for immunotherapy. It is important to note that there are differences in how the terms “extensively tested” or “understudied” are determined. A PubMed review of over 1000 citations pertaining to cancer and immunotherapy showed a significantly greater number of original published works related to immunotherapy for melanoma and lung cancer than for other cancer types (Figure 1). However, a review of over 500 clinical trials in ClinicalTrials.gov involving immunological interventions for cancer patients revealed lung cancer and, instead of melanoma, breast cancer to be the most common cancers being targeted (Figure 2). While clinical trials involving immunological interventions for patients with pancreatic and ovarian cancers appeared at a high frequency in ClinicalTrials.gov (Available online: https://clinicaltrials.gov/), published results involving such trials were more rare compared to results studies involving of immunotherapies for patients with other cancer types. The focus of this special edition has been on cancers that have received more limited attention as targets for immunotherapy or for which new immunological approaches have lagged or been stagnant. Below (Table 1) is a summary of the original research articles that represent this Special Issue entitled “Cancer Immunology with a Focus on Understudied Cancers as Targets for Immunotherapy” in International Journal of Molecular Sciences. In addition to these original research papers, the Special Issue also contains a number of review papers exploring new immunological treatment targets [8] and treatment approaches for lung cancer [9], multiple myeloma [10], ovarian cancer [11] and colorectal cancer [12]. It is recognized cancers should not all be lumped into a single category as they express different antigens and establish microenvironments that differ, in part based on the cancer location and the immune modulators that they express. The challenges of immunotherapy have been a topic of interest and have recently extensive reviews in the literature [13,14,15,16,17,18]. Some exhibit more profound levels of immune suppression than others, thereby increasing the challenge of immunotherapeutic strategies. Others show more inflammatory phenotypes. However, lessons learned from immunological treatments for one cancer type can be used to help guide treatment approaches for other cancer types. It is hoped that immunological treatments that have been tested and shown to be effective for cancers that have been more frequently studied can be tested in cancers that have less frequently been considered for immunotherapy. It is also hoped that the studies described in this special edition can readily wind their way from diagnostic approaches to identification of new target antigens, in vitro feasibility analyses, in vivo studies in orthotopic animal models and, finally, to cancer patients.

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          Most cited references17

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          Advances in Cancer Immunotherapy in Solid Tumors

          Immunotherapy is heralded as one of the most important advances in oncology. Until recently, only limited immunotherapeutic options were available in selected immunogenic cancers like melanoma and renal cell carcinomas. Nowadays, there is an improved understanding that anti-tumor immunity is controlled by a delicate balance in the tumor microenvironment between immune stimulatory and immune inhibitory pathways. Either by blocking the inhibitory pathways or stimulating the activating pathways that regulate cytotoxic lymphocytes, anti-tumor immunity can be enhanced leading to durable anti-tumor responses. Drugs which block the immune regulatory checkpoints namely the PD-1/PDL1 and CTLA 4 pathway have shown tremendous promise in a wide spectrum of solid and hematological malignancies, significantly improving overall survival in newly diagnosed and heavily pretreated patients alike. Hence there is renewed enthusiasm in the field of immune oncology with current research focused on augmenting responses to checkpoint inhibitors by combination therapy as well as studies looking at other immune modulators and adoptive T cell therapy. In this article, we highlight the key clinical advances and concepts in immunotherapy with particular emphasis on checkpoint inhibition as well as the future direction in this field.
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            Targeting the Tumor Microenvironment: The Protumor Effects of IL-17 Related to Cancer Type

            The inflammatory process contributes to immune tolerance as well as to tumor progression and metastasis. By releasing extracellular signals, cancerous cells constantly shape their surrounding microenvironment through their interactions with infiltrating immune cells, stromal cells and components of extracellular matrix. Recently, the pro-inflammatory interleukin 17 (IL-17)-producing T helper lymphocytes, the Th17 cells, and the IL-17/IL-17 receptor (IL-17R) axis gained special attention. The IL-17 family comprises at least six members, IL-17A, IL-17B, IL-17C, IL-17D, IL-17E (also called IL-25), and IL-17F. Secreted as disulfide-linked homo- or heterodimers, the IL-17 bind to the IL-17R, a type I cell surface receptor, of which there are five variants, IL-17RA to IL-17RE. This review focuses on the current advances identifying the promoting role of IL-17 in carcinogenesis, tumor metastasis and resistance to chemotherapy of diverse solid cancers. While underscoring the IL-17/IL-17R axis as promising immunotherapeutic target in the context of cancer managing, this knowledge calls upon further in vitro and in vivo studies that would allow the development and implementation of novel strategies to combat tumors.
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              Hypoxia Inducible Factor 1 (HIF-1) Recruits Macrophage to Activate Pancreatic Stellate Cells in Pancreatic Ductal Adenocarcinoma

              Hypoxia inducible factor 1 (HIF-1) is a transcription factor composed of two subunits, namely, HIF-1α and HIF-1β, in which HIF-1β is constitutively expressed. HIF-1 upregulates several hypoxia-responsive proteins, including angiogenesis factors, glycolysis solution enzymes, and cell survival proteins. HIF-1 is also associated with the degree of inflammation in the tumor region, but the exact mechanism remains unclear. This study aims to identify the molecular mechanism of recruiting monocytes/macrophages by HIF-1α in pancreatic ductal adenocarcinoma (PDAC) and the effects of macrophages on pancreatic stellate cells (PSCs). Immunohistochemistry (IHC) was performed for cluster of differentiation 68 (CD68), HIF-1α, and chemical chemokines 2 (CCL2). Western blot, real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR), chromatin immunoprecipitation assay, and The Cancer Genome Atlas (TCGA) were used to verify the correlation between HIF-1α and CCL2 at protein and nucleic acid levels. Monocytes/macrophages were co-cultured with PSCs to observe their interaction. Samples showed significant correlation between CD68 and HIF-1α (t-test, p < 0.05). HIF-1α recruited monocytes/macrophages by promoting CCL2 secretion. Moreover, macrophages could accelerate the activation of PSCs. HIF-1α might promote inflammation and fibrosis of PDAC through CCL2 secretion, which may provide a novel target to treat PDAC patients.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                11 January 2017
                January 2017
                : 18
                : 1
                : 127
                Affiliations
                [1 ]Research Service (151), Ralph H. Johnson Veterans Affairs Medical Center, 109 Bee Street, Charleston, SC 29401, USA; rita.young@ 123456va.gov ; Tel.: +1-843-792-9953
                [2 ]Department of Otolaryngology—Head and Neck Surgery, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29425, USA
                Article
                ijms-18-00127
                10.3390/ijms18010127
                5297761
                28085027
                930538d0-b503-4549-975f-5667ddbd6398
                © 2017 by the author; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 October 2016
                : 08 December 2016
                Categories
                Editorial

                Molecular biology
                Molecular biology

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