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Genomics meets immunity in pancreatic cancer: Current research and future directions for pancreatic adenocarcinoma immunotherapy 癌症基因组学与免疫的结合:胰腺癌免疫治疗的研究现状和未来方向
IF 3.6
Oncology Reviews Pub Date : 2019-07-22 DOI: 10.4081/oncol.2019.430
Jacob S. Bowers, Stefanie R. Bailey, M. Rubinstein, C. Paulos, E. Camp
{"title":"Genomics meets immunity in pancreatic cancer: Current research and future directions for pancreatic adenocarcinoma immunotherapy","authors":"Jacob S. Bowers, Stefanie R. Bailey, M. Rubinstein, C. Paulos, E. Camp","doi":"10.4081/oncol.2019.430","DOIUrl":"https://doi.org/10.4081/oncol.2019.430","url":null,"abstract":"Pancreatic adenocarcinoma (PDAC) remains a formidable disease that needs improved therapeutic strategies. Even though immunotherapy has revolutionized treatment for various solid tumor types, it remains largely ineffective in treating individuals with PDAC. This review describes how the application of genome-wide analysis is revitalizing the field of PDAC immunotherapy. Major themes include new insights into the body’s immune response to the cancer, and key immunosuppressive elements that blunt that antitumor immunity. In particular, new evidence indicates that T cell-based antitumor immunity against PDAC is more common, and more easily generated, than previously thought. However, equally common are an array of cellular and molecular defenses employed by the tumor against those T cells. These discoveries have changed how current immunotherapies are deployed and have directed development of novel strategies to better treat this disease. Thus, the impact of genomic analysis has been two-fold: both in demonstrating the heterogeneity of immune targets and defenses in this disease, as well as providing a powerful tool for designing and identifying personalized therapies that exploit each tumor’s unique phenotype. Such personalized treatment combinations may be the key to developing successful immunotherapies for pancreatic adenocarcinoma.","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":" ","pages":""},"PeriodicalIF":3.6,"publicationDate":"2019-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.430","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46867961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Prognostic significance of mutated genes in megakaryocytic disorders 突变基因在巨核细胞疾病中的预后意义
IF 3.6
Oncology Reviews Pub Date : 2019-07-22 DOI: 10.4081/oncol.2019.408
A. Asnafi, M. Mohammadi, Hadi Rezaeeyan, Nader Davari, N. Saki
{"title":"Prognostic significance of mutated genes in megakaryocytic disorders","authors":"A. Asnafi, M. Mohammadi, Hadi Rezaeeyan, Nader Davari, N. Saki","doi":"10.4081/oncol.2019.408","DOIUrl":"https://doi.org/10.4081/oncol.2019.408","url":null,"abstract":"Megakaryopoiesis is a process during which platelets that play a major role in hemostasis are produced due to differentiation and maturation of megakaryocytic precursors. Several genes, including oncogenes and tumor suppressor genes, play a role in the regulation of this process. This study was conducted to investigate the oncogenes and tumor suppressor genes as well as their mutations during the megakaryopoiesis process, which can lead to megakaryocytic disorders. Relevant literature was identified by a PubMed search (1998-2019) of English language papers using the terms ‘Megakaryopoiesis’, ‘Mutation’, ‘oncogenes’, and ‘Tumor Suppressor’. According to investigations, several mutations occur in the genes implicated in megakaryopoiesis, which abnormally induce or inhibit megakaryocyte production, differentiation, and maturation, leading to platelet disorders. GATA-1 is one of the important genes in megakaryopoiesis and its mutations can be considered among the factors involved in the incidence of these disorders. Considering the essential role of these genes (such as GATA- 1) in megakaryopoiesis and the involvement of their mutations in platelet disorders, study and examination of these changes can be a positive step in the diagnosis and prognosis of these diseases.","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":" ","pages":""},"PeriodicalIF":3.6,"publicationDate":"2019-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.408","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45253034","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
CDK4/6 inhibitors in advanced breast cancer, what is beyond? CDK4/6抑制剂在晚期乳腺癌中的作用?
IF 3.6
Oncology Reviews Pub Date : 2019-07-22 DOI: 10.4081/oncol.2019.416
Amrallah A. Mohammed, Hanaa Rashied, F. M. Elsayed
{"title":"CDK4/6 inhibitors in advanced breast cancer, what is beyond?","authors":"Amrallah A. Mohammed, Hanaa Rashied, F. M. Elsayed","doi":"10.4081/oncol.2019.416","DOIUrl":"https://doi.org/10.4081/oncol.2019.416","url":null,"abstract":"Resistant to hormonal treatment considered the main clinical challenge in the management of advanced breast cancer (ABC). The use of CDK4/6 inhibitors (CDK4/6I) may change the treatment landscape. In this mandated review, we will focus on the applicable role of CDK4/6I in the management of HR+/HER2- ABC, mechanisms of resistance, and promising future implementation.","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":" ","pages":""},"PeriodicalIF":3.6,"publicationDate":"2019-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.416","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43484784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Thrombocytopenia in solid tumors: Prognostic significance. 实体瘤中的血小板减少症:预后意义。
IF 3.1
Oncology Reviews Pub Date : 2019-05-14 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.413
Majid Ghanavat, Mina Ebrahimi, Hassan Rafieemehr, Mahmood Maniati, Masumeh Maleki Behzad, Saeid Shahrabi
{"title":"Thrombocytopenia in solid tumors: Prognostic significance.","authors":"Majid Ghanavat, Mina Ebrahimi, Hassan Rafieemehr, Mahmood Maniati, Masumeh Maleki Behzad, Saeid Shahrabi","doi":"10.4081/oncol.2019.413","DOIUrl":"10.4081/oncol.2019.413","url":null,"abstract":"<p><p>Solid tumors are a heterogeneous group of malignancies that result from out-of-control proliferation of cells. Thrombocytopenia is a common complication among patients with solid tumors that predispose them to bleeding disorders. The aim of this review article is to investigate the underlying mechanisms of the risk and incidence of thrombocytopenia in solid tumors. It can be argued that thrombocytopenia is a poor prognostic factor in solid tumors that can result from several factors such as polymorphism and mutation in some transcription factors and cytokines involved in megakaryocytic maturation or from the adverse effects of treatment. Therefore, an understanding of the exact mechanism of thrombocytopenia pathogenesis in each stage of solid tumors can help in developing therapeutic strategies to decrease bleeding complications in these malignancies.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"413"},"PeriodicalIF":3.1,"publicationDate":"2019-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7c/00/onco-13-1-413.PMC6542370.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37061071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prognostic significance of aberrant CD5 expression in B-cell leukemia. CD5异常表达在b细胞白血病中的预后意义。
IF 3.6
Oncology Reviews Pub Date : 2019-04-18 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.400
Kaveh Jaseb, Daryush Purrahman, Saeid Shahrabi, Majid Ghanavat, Hadi Rezaeean, Najmaldin Saki
{"title":"Prognostic significance of aberrant CD5 expression in B-cell leukemia.","authors":"Kaveh Jaseb,&nbsp;Daryush Purrahman,&nbsp;Saeid Shahrabi,&nbsp;Majid Ghanavat,&nbsp;Hadi Rezaeean,&nbsp;Najmaldin Saki","doi":"10.4081/oncol.2019.400","DOIUrl":"https://doi.org/10.4081/oncol.2019.400","url":null,"abstract":"<p><p>Aberrant expression of CD5 (as a T-cell marker) is seen in some leukemia and lymphoma of B lineage origin. Given that the signaling resulting from the expression of this marker plays an essential role in the development of leukemia and lymphoma, evaluating the expression of this marker is of paramount importance. Therefore, our goal in this study was to investigate the prognostic importance of CD5 expression in B-cell leukemia and lymphoma. We evaluate CD5 expression in normal and leukemic B-cells by identifying relevant literature through a PubMed search (1998-2018) of English language papers using the terms: '<i>CD5,' 'B-cell,' 'Leukemia</i>,' and <i>'Lymphoma.</i>' We are doing this thorough comparison of results from CD5 positive and negative cases to make a correct decision about prognostic importance of CD5 expression in these malignancies. In a number of B-cell malignancies, CD5 is expressed in varying degrees. Due to the different origins and characteristics of these malignancies, the results of CD5 expression evaluations are heterogeneous and impossible to generalize. However, CD5 expression is sometimes associated with clinicopathologic findings, more invasive clinical course, and even resistance to treatment (specifically in DLBCL) among CD5- positive patients, which appears to be a function of CD5 signaling and its downstream factors such as STAT3. Depending on the type of malignancy, CD5 expression is associated with good or bad prognosis, which can be used as an auxiliary prognostic factor to assess the clinical course of B-cell malignancies. Moreover, the difference in expression levels of CD5 in a variety of B-cell malignancies allows for differential diagnosis of these malignancies, which can be helpful when diagnosis is difficult.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"400"},"PeriodicalIF":3.6,"publicationDate":"2019-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.400","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37204652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Prospects for repurposing CNS drugs for cancer treatment. 中枢神经系统药物用于癌症治疗的前景。
IF 3.6
Oncology Reviews Pub Date : 2019-04-17 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.411
Mohamed Abdelaleem, Hossam Ezzat, Muhammed Osama, Adel Megahed, Waleed Alaa, Ahmed Gaber, Ayman Shafei, Alaa Refaat
{"title":"Prospects for repurposing CNS drugs for cancer treatment.","authors":"Mohamed Abdelaleem,&nbsp;Hossam Ezzat,&nbsp;Muhammed Osama,&nbsp;Adel Megahed,&nbsp;Waleed Alaa,&nbsp;Ahmed Gaber,&nbsp;Ayman Shafei,&nbsp;Alaa Refaat","doi":"10.4081/oncol.2019.411","DOIUrl":"https://doi.org/10.4081/oncol.2019.411","url":null,"abstract":"Drug repurposing is the idea of using an already approved drug for another disease or disorder away from its initial use. This new approach ensures the reduction in high cost required for developing a new drug in addition to the time consumed, especially in the tumor disorders that show an unceasing rising rate with an unmet success rate of new anticancer drugs. In our review, we will review the anti-cancer effect of some CNS drugs, including both therapeutic and preventive, by searching the literature for preclinical or clinical evidence for anticancer potential of central nervous system drugs over the last 8 years period (2010-2018) and including only evidence from Q1 journals as indicated by Scimago website (www.scimagojr.com). We concluded that Some Central Nervous system drugs show a great potential as anti-cancer in vitro, in vivo and clinical trials through different mechanisms and pathways in different types of cancer that reveal a promising evidence for the repurposing of CNS drugs for new indications.","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"411"},"PeriodicalIF":3.6,"publicationDate":"2019-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.411","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37204656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
Adherence to oral pharmacological treatment in cancer patients: Systematic review. 癌症患者口服药物治疗的依从性:系统评价。
IF 3.6
Oncology Reviews Pub Date : 2019-04-16 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.402
Melissa Perdomo Claros, Claudia Viviana Marín Messa, Herney Andrés García-Perdomo
{"title":"Adherence to oral pharmacological treatment in cancer patients: Systematic review.","authors":"Melissa Perdomo Claros,&nbsp;Claudia Viviana Marín Messa,&nbsp;Herney Andrés García-Perdomo","doi":"10.4081/oncol.2019.402","DOIUrl":"https://doi.org/10.4081/oncol.2019.402","url":null,"abstract":"<p><p>The objective was to identify the best-validated scale for assessing oral pharmacological adherence in oncology patients. A bibliographic search was performed in MEDLINE via Ovid, EMBASE, CENTRAL and LILACS. We included all studies in which a validation of adherence scales to oral pharmacological treatment was performed in oncology patients older than 18 years without gender distinction. We excluded studies that included newly diagnosed patients. No statistical analysis was performed due to the nature of the study. A total of 4609 studies were found. After screening, six studies were selected for qualitative analysis. In the analysis of the six included studies, a total of 855 patients older than 18 years with oncological diagnoses were found. Two of the studies, Bagcivan <i>et al</i>. and Amorim <i>et al</i>., used scales that show acceptable validity and reliability to adequately measure adherence to pharmacological treatment in each of the patients. In this way, the quality of patient care and success in pharmacological treatments can be guaranteed. According to the results obtained in the evaluation of biases and analysis of psychometric properties, the best-validated scales are as follows: Adherence Determinants Questionnaire (ADQ) (Brazilian version) and the Oral Chemotherapy Adherence Scale (OCAS). These are valid, reliable and useful scales that can be adapted to any cultural context.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"402"},"PeriodicalIF":3.6,"publicationDate":"2019-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.402","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37204653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
A comprehensive overview of mitochondrial DNA 4977-bp deletion in cancer studies. 线粒体DNA 4977-bp缺失在癌症研究中的全面概述。
IF 3.6
Oncology Reviews Pub Date : 2019-04-16 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.409
Abdul Aziz Mohamed Yusoff, Wan Salihah Wan Abdullah, Siti Zulaikha Nashwa Mohd Khair, Siti Muslihah Abd Radzak
{"title":"A comprehensive overview of mitochondrial DNA 4977-bp deletion in cancer studies.","authors":"Abdul Aziz Mohamed Yusoff,&nbsp;Wan Salihah Wan Abdullah,&nbsp;Siti Zulaikha Nashwa Mohd Khair,&nbsp;Siti Muslihah Abd Radzak","doi":"10.4081/oncol.2019.409","DOIUrl":"https://doi.org/10.4081/oncol.2019.409","url":null,"abstract":"<p><p>Mitochondria are cellular machines essential for energy production. The biogenesis of mitochondria is a highly complex and it depends on the coordination of the nuclear and mitochondrial genome. Mitochondrial DNA (mtDNA) mutations and deletions are suspected to be associated with carcinogenesis. The most described mtDNA deletion in various human cancers is called the 4977-bp common deletion (mDNA<sup>4977</sup>) and it has been explored since two decades. In spite of that, its implication in carcinogenesis still unknown and its predictive and prognostic impact remains controversial. This review article provides an overview of some of the cellular and molecular mechanisms underlying mDNA<sup>4977</sup> formation and a detailed summary about mDNA<sup>4977</sup> reported in various types of cancers. The current knowledges of mDNA<sup>4977</sup> as a prognostic and predictive marker are also discussed.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"409"},"PeriodicalIF":3.6,"publicationDate":"2019-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.409","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37204654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 32
Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility. 骨髓增生异常综合征的复杂核型:诊断程序和预后易感性。
IF 3.6
Oncology Reviews Pub Date : 2019-02-04 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.389
Mohammad Shahjahani, Elham Homaei Hadad, Shirin Azizidoost, Kowsar Chenani Nezhad, Saeid Shahrabi
{"title":"Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility.","authors":"Mohammad Shahjahani,&nbsp;Elham Homaei Hadad,&nbsp;Shirin Azizidoost,&nbsp;Kowsar Chenani Nezhad,&nbsp;Saeid Shahrabi","doi":"10.4081/oncol.2019.389","DOIUrl":"https://doi.org/10.4081/oncol.2019.389","url":null,"abstract":"<p><p>Complex karyotype (CK) is a poor prognosis factor in hematological malignancies. Studies have shown that the presence of CK in myelodysplastic syndrome (MDS) can be associated with MDS progression to acute myeloid leukemia. The goal of this review was to examine the relationship between different types of CK with MDS, as well as its possible role in the deterioration and progression of MDS to leukemia. The content used in this paper has been obtained by a PubMed and Google Scholar search of English language papers (1975-2018) using the terms <i>complex karyotype</i> and <i>myelodysplastic syndromes</i>. A single independent abnormality can be associated with a good prognosis. However, the coexistence of a series of abnormalities can lead to CK, which is associated with the deterioration of MDS and its progression to leukemia. Therefore, CK may be referred to as a prognostic factor in MDS. The detection of independent cytogenetic disorders that altogether can result in CK could be used as a prognostic model for laboratory and clinical use.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"389"},"PeriodicalIF":3.6,"publicationDate":"2019-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.389","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37045058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Advances in pancreatic cancer biomarkers. 胰腺癌生物标志物研究进展
IF 3.6
Oncology Reviews Pub Date : 2019-02-01 eCollection Date: 2019-01-14 DOI: 10.4081/oncol.2019.410
Syed Hasan, Rojymon Jacob, Upender Manne, Ravi Paluri
{"title":"Advances in pancreatic cancer biomarkers.","authors":"Syed Hasan,&nbsp;Rojymon Jacob,&nbsp;Upender Manne,&nbsp;Ravi Paluri","doi":"10.4081/oncol.2019.410","DOIUrl":"https://doi.org/10.4081/oncol.2019.410","url":null,"abstract":"<p><p>Biomarkers play an essential role in the management of patients with invasive cancers. Pancreatic ductal adenocarcinoma (PDC) associated with poor prognosis due to advanced presentation and limited therapeutic options. This is further complicated by absence of validated screening and predictive biomarkers for early diagnosis and precision treatments respectively. There is emerging data on biomarkers in pancreatic cancer in past two decades. So far, the CA 19-9 remains the only approved biomarker for diagnosis and response assessment but limited by low sensitivity and specificity. In this article, we aim to review current and future biomarkers that has potential serve as critical tools for early diagnostic, predictive and prognostic indications in pancreatic cancer.</p>","PeriodicalId":19487,"journal":{"name":"Oncology Reviews","volume":"13 1","pages":"410"},"PeriodicalIF":3.6,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4081/oncol.2019.410","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37204655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 82
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