摘要
背景:胰腺导管腺癌(PDAC)是破坏性的。由于其沉默性质,一旦达到高级,经常不能手术的阶段,该疾病通常被诊断出来。迄今为止,我们没有促进早期诊断的生物标志物,留下足够的时间进行治疗性治疗,有效降低了该癌症实体的非常高的死亡率。因此,PDAC患者的预期寿命较低(即5年生存率≤6%)。包括PDAC肿瘤基质特征和特征的新数据可能会更好地解释其侵袭性,相对持久的无痛扩张以及为何化疗如此频繁失败。典型的肿瘤诱导的基质细胞增生症的特征是与癌症相关的成纤维细胞(CAF),免疫监视减少,癌症相关的神经重塑和非常低的血管密度。这种基质微环境产生缺氧,营养缺乏,免疫抑制和化学耐药性。这些因素的结合导致了一种恶性疾病,从大肿瘤块的长期,无症状发展开始,其后是高百分比的不可手术状态的延迟诊断,对所有保守治疗方案(包括辐射)表现出差的反应,其结束转移导致快速的致命结果。 目的:在本文中,我们回顾了PDAC组织的遗传,细胞,免疫学,纳米医学和基质特征的联系,并讨论与肿瘤进展速率相关和/或之前的代谢异常。 结论:对基础机制的更全面的了解可以改善患有这种破坏性癌症的患者的诊断和治疗管理。
关键词: 胰腺导管腺癌,基质pdac细胞相互作用的新见解,神经重塑方面,免疫学方面,代谢方面,遗传方面,纳米医学方面。
Current Medicinal Chemistry
Title:New Diagnostic and Therapeutic Aspects of Pancreatic Ductal Adenocarcinoma
Volume: 24 Issue: 28
关键词: 胰腺导管腺癌,基质pdac细胞相互作用的新见解,神经重塑方面,免疫学方面,代谢方面,遗传方面,纳米医学方面。
摘要: Background: Pancreatic ductal adenocarcinoma (PDAC) is devastating. Because of its silent nature, the disease is often only diagnosed once it has reached an advanced, frequently inoperable stage. To date, we have no biomarkers that facilitate earlier diagnosis, leaving sufficient time for curative therapy that effectively lowers the very high mortality rate of this cancer entity. Because of this, the life expectancy of patients with PDAC is low (i.e. ≤ 6% five-year survival rates). New data, including particular genetic signatures and features of the stromal architecture of PDAC tumors, may better explain their aggressiveness, their relatively long-lasting painless expansion, and why chemotherapy so frequently fails. The typical tumor-induced stromal desmoplasia is characterized by cancer-associated fibroblasts (CAFs), decreased immune surveillance, cancer-associated neural remodeling, and a very low vascular density. This stromal microenvironment generates hypoxia, nutrient deficiency, immune suppression, and chemoresistance. The combination of factors results in a vicious disease that begins with the long-lasting, asymptomatic development of a large tumor mass, followed by a delayed diagnosis with a high percentage of inoperable states, exhibiting a poor response to all conservative therapeutic options, including radiation, and which ends with metastasis resulting in a rapid fatal outcome.
Objective: In this article, we review coherences on genetic, cellular, immunological, Nano medical and stromal characteristics of PDAC tissue, and discuss metabolic abnormalities associated with and/or preceding the tumor progression rate.
Conclusion: A more comprehensive understanding of the underlying mechanisms can improve the diagnostic and therapeutic management of patients suffering from this devastating type of cancer.
Export Options
About this article
Cite this article as:
New Diagnostic and Therapeutic Aspects of Pancreatic Ductal Adenocarcinoma, Current Medicinal Chemistry 2017; 24 (28) . https://dx.doi.org/10.2174/0929867324666170510150124
DOI https://dx.doi.org/10.2174/0929867324666170510150124 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements
Related Articles
-
Dietary Manipulation of Precursor Polyunsaturated Fatty Acids Modulates Eicosanoid and Endocannabinoid Synthesis: A Potential Tool to Control Tumor Development
Current Nutrition & Food Science Editorial (Thematic Issue: Metabolic Disorders, Drug Development, Drug Design and Biomarkers)
Current Pharmaceutical Design An Update on Molecular Research of Pancreatic Adenocarcinoma
Anti-Cancer Agents in Medicinal Chemistry Interconnection of Estrogen/Testosterone Metabolism and Mevalonate Pathway in Breast and Prostate Cancers
Current Molecular Pharmacology Clinical Applications of the Urokinase Receptor (uPAR) for Cancer Patients
Current Pharmaceutical Design Emerging Opportunities and Concerns for Drug Discovery at Serotonin 5-5-HT2B Receptors
Current Topics in Medicinal Chemistry Light Directed Gene Transfer by Photochemical Internalisation
Current Gene Therapy Therapeutic Angiogenesis for Islet Revascularization
Immunology, Endocrine & Metabolic Agents in Medicinal Chemistry (Discontinued) Inhibitors of the Microsomal Prostaglandin E2 Synthase-1 as Alternative to Non Steroidal Anti-Inflammatory Drugs (NSAIDs) – A Critical Review
Current Medicinal Chemistry Development of Natural Bioactive Alkaloids: Anticancer Perspective
Mini-Reviews in Medicinal Chemistry The Effects of Nanoencapsulated Curcumin-Fe3O4 on Proliferation and hTERT Gene Expression in Lung Cancer Cells
Anti-Cancer Agents in Medicinal Chemistry Synthetic Peptides Derived from the C-Terminal Region of Lys49 Phospholipase A2 Homologues from Viperidae Snake Venoms: Biomimetic Activities and Potential Applications
Current Pharmaceutical Design Radiolabelled Probes Targeting Infection and Inflammation for Personalized Medicine
Current Pharmaceutical Design Thymoquinone: Major Molecular Targets, Prominent Pharmacological Actions and Drug Delivery Concerns
Current Bioactive Compounds New Pharmacological Perspectives and Therapeutic Potential of PPAR-γ Agonists
Current Pharmaceutical Design Current and Potential Anticancer Drugs Targeting Members of the UHRF1 Complex Including Epigenetic Modifiers
Recent Patents on Anti-Cancer Drug Discovery Role of Lipoxins and Resolvins as Anti-Inflammatory and Proresolving Mediators in Colon Cancer
Current Molecular Medicine The Quest for Novel Biomarkers in Early Diagnosis of Diabetic Neuropathy
Current Proteomics Updates of mTOR Inhibitors
Anti-Cancer Agents in Medicinal Chemistry A Direct Interaction Between Mitochondrial Proteins and Amyloid-β Peptide and its Significance for the Progression and Treatment of Alzheimer’s Disease
Current Medicinal Chemistry