A prognostic signature based on immune-related genes for cervical squamous cell carcinoma and endocervical adenocarcinoma

Cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) is the fourth commonest female malignancy worldwide. CESC progresses in immune-microenvironment mainly composed of infiltrating immune and stromal cells. Here, we performed an integrated analysis incorporating the expression profiles from the Cancer Genome Atlas (TCGA) database and scores of immune and stromal cells calculated by Estimation of Stromal and Immune cells in Malignant Tumours using Expression data (ESTIMATE) algorithm. A two-gene signature (CD1C and CD6 genes) was established to predict the prognosis of CESC. Based on this signature, patients were divided into the high- and low-risk groups, and this signature showed good prognostic performance according to the results of Kaplan-Meier analysis and receiver operating characteristic (ROC) analysis in train set and two validation sets. A nomogram was built for evaluating the clinical applicability of this signature. In addition, based on Tumor Immune Estimation Resource (TIMER) database, 2 hub genes showed negative correlations with tumor purity and positive correlations with infiltrating levels of immune filtrating cells. What’s more, we propose new treatment strategies for the two prognostic subtypes. Low- risk patients were found presenting with a higher level of immune checkpoint molecules and showing higher immunogenicity in immunophenoscore (IPS) analysis, which indicated a better response for immunotherapy. Meanwhile, estimated by Genomics of Drug Sensitivity in Cancer (GDSC) database, the high-risk patients showed sensitive responses to five chemotherapy drugs. Finally, 10 candidate small-molecule drugs for CESC were defined. In summary, the CD1C-CD6 signature can accurately predict the prognosis of CESC.     

奥美拉唑的不良反应及其与其他药物间的相互作用研究

目的探究奥美拉唑所引起的不良反应及其与其他药物间的相互作用。方法122例接受奥美拉唑治疗并出现不良反应的患者,分析患者所处的环境状况、情绪状况、过敏史、年龄、过敏体质、生活习惯、饮酒情况等临床资料,探讨不良反应的发生原因,并分析不良反应累及系统分布情况及临床症状、导致不良反应的药物使用类型以及预后情况。结果122例奥美拉唑所致不良反应患者中,男性患者、年龄40~50岁、过敏体质、过敏史、情绪不稳定、药后饮酒、环境状况差占比相对较高。122例患者奥美拉唑所致不良反应中免疫系统占27.87%、消化道系统占23.77%、心脑血管系统占7.38%、神经系统占9.02%、血液系统占21.31%、肝胆系统占10.66%。患者常见临床症状为皮疹、瘙痒、皮炎、过敏性休克、恶心、呕吐、腹泻、心动过速、心律不齐、头晕、头痛、意识模糊、血小板下降、白细胞减少、血尿、肝功能障碍等。奥美拉唑与抗癫痫药苯妥英、抗惊厥药卡马西平、抗焦虑抗癫痫药地西泮以及安替比林药物相互作用,会使机体代谢功能降低,其发生可能与抑制钠离子内流有关。结论奥美拉唑所致不良反应会累及机体多个系统,因此医护人员应加强对患者的问诊,了解患者的相关情况,设计合理的用药方案,减少不良反应的发生。     

luminal型乳腺癌患者戈舍瑞林用药依从性现状及影响因素分析

目的了解luminal型乳腺癌患者戈舍瑞林用药依从性情况，分析影响其依从性的相关因素。 方法根据纳入及排除标准，收集2015年1月至2017年12月重庆医科大学附属第一医院内分泌乳腺外科使用戈舍瑞林治疗的luminal型乳腺癌女性患者174例进行回顾性分析。中位随访时间16个月(范围：1～54个月)，完成随访154例，失访20例，失访率为11.5%(20/174)。采用问卷调查评价其用药依从性，使用χ²检验和Mann-Whitney U检验比较不同特征患者依从性的差异；用Logistic回归分析影响患者依从性的相关因素。将患者分为≤40岁(103例)和>40岁(51例)2个亚组，进行亚组分析。 结果在完成随访的154例患者中，依从性好82例(53.2%，82/154)，依从性差72例(46.8%，72/154)。≤40岁组患者中，55.3%(57/103)依从性好，而>40岁组患者中仅49.0%(25/51)依从性好。全部患者中，文化程度、医保类型、不良反应和是否了解疗程时间均与乳腺癌患者戈舍瑞林用药依从性有关(χ²＝13.586、13.042、7.880、14.251，P均<0.050)；Logistic回归分析结果显示：高中及以下学历、居民医保和不了解戈舍瑞林的疗程时间为影响依从性的危险因素(OR＝2.772，95%CI：1.243～6.183，P＝0.013；OR＝5.188，95%CI：1.383～19.465，P＝0.015; OR＝3.363，95%CI：1.645～6.878，P＝0.001)。亚组分析显示：文化程度、职业、医保类型和是否了解疗程时间是≤40岁患者戈舍瑞林用药依从性的影响因素(χ²＝15.992、5.978、7.701、10.376，P均<0.050)；不良反应及医保类型是>40岁患者用药依从性的影响因素(χ²＝4.763、7.471，P均<0.050)。Logistic回归分析表明：高中及以下文化程度和不了解疗程时间是≤40岁患者用药依从性的危险因素(OR＝5.126，95%CI：2.086～12.598，P<0.001; OR＝3.631, 95%CI：1.500～8.792，P＝0.004)；居民医保是>40岁患者用药依从性的危险因素(OR＝64.315，95%CI：2.513～1 646.042，P＝0.012)，不良反应是>40岁患者用药依从性的保护因素OR＝0.189，95%CI＝0.047～0.759，P＝0.019)。 结论luminal型乳腺癌患者戈舍瑞林用药依从性较差，文化程度、医保类型及是否了解疗程时间都可能影响患者的依从性。≤40岁组和>40岁组患者依从性有差异，且影响因素不同，建议对不同年龄患者用药采用不同的干预措施。     

uPAR Controls Vasculogenic Mimicry Ability Expressed by Drug-Resistant Melanoma Cells

Malignant melanoma is a highly aggressive skin cancer characterized by an elevated grade of tumor cell plasticity. Such plasticity allows adaptation of melanoma cells to different hostile conditions and guarantees tumor survival and disease progression, including aggressive features such as drug resistance. Indeed, almost 50% of melanoma rapidly develop resistance to the BRAFV600E inhibitor vemurafenib, with fast tumor dissemination, a devastating consequence for patients’ outcomes. Vasculogenic mimicry (VM), the ability of cancer cells to organize themselves in perfused vascular-like channels, might sustain tumor spread by providing vemurafenibresistant cancer cells with supplementary ways to enter into circulation and disseminate. Thus, this research aims to determine if vemurafenib resistance goes with the acquisition of VM ability by aggressive melanoma cells, and identify a driving molecule for both vemurafenib resistance and VM. We used two independent experimental models of drug-resistant melanoma cells, the first one represented by a chronic adaptation of melanoma cells to extracellular acidosis, known to drive a particularly aggressive and vemurafenib-resistant phenotype, the second one generated with chronic vemurafenib exposure. By performing in vitro tube formation assay and evaluating the expression levels of the VM markers EphA2 and VE-cadherin by Western blotting and flow cytometer analyses, we demonstrated that vemurafenib-resistant cells obtained by both models are characterized by an increased ability to perform VM. Moreover, by exploiting the CRISPR-Cas9 technique and using the urokinase plasminogen activator receptor (uPAR) inhibitor M25, we identified uPAR as a driver of VM expressed by vemurafenib-resistant melanoma cells. Thus, uPAR targeting may be successfully leveraged as a new complementary therapy to inhibit VM in drug-resistant melanoma patients, to counteract the rapid progression and dissemination of the disease.     

Impact of pharmaceutical price controls on the cost of cardiovascular drugs: does essentiality matter?

ABSTRACT

Background

With the goal of improving the affordability of medicines, governments across the globe have instituted various forms of price controls. Since 2013, India has been regulating the prices of drugs included in its national list of essential medicines (NLEM). Here we evaluate the cost variations among available cardiovascular drugs and perform cost-analysis comparing essential and non-essential drugs.     

社区获得性肺炎的中西医治疗研究进展

社区获得性肺炎(Community Acquired Pneumonia,CAP)是比较常见的院外肺部炎性疾病之一,随着细菌、支原体、衣原体等多种病原体的耐药率的上升,以及病患梯度的范围增加,CAP的发病率呈逐年上升的趋势,死亡率日益增高,导致医疗资源消耗巨大。目前临床上CAP的患者主要依靠经验性治疗。正确选择抗生素、减少病原体的耐药率,优化肺部炎症疾病的医疗方案,提高CAP临床治愈率已经成为临床医生当前面临的一项重大挑战。中药制剂具有广谱抗菌、调节免疫、不易耐药、简便价廉等特点,是解决上述难题的一个很好途径。     

US Food and Drug Administration approvals for Bruton tyrosine kinase inhibitors in patients with chronic lymphocytic leukemia: Potential inefficiencies in trial design and evidence generation

The US Food and Drug Administration granted acalabrutinib approval as the second Bruton tyrosine kinase (BTK) inhibitor to treat patients with chronic lymphocytic leukemia and small lymphocytic lymphoma as monotherapy or in combination with obinutuzumab. This approval was based on 2 phase 3 trials: ELEVATE-TN and ASCEND. There are several concerns with the design of these trials, including suboptimal treatment of patients in the control arm, expansion of the trial population, and lack of data regarding efficacy or tolerability compared with ibrutinib, a first-in-class drug. The Food and Drug Administration approval of acalabrutinib for patients with chronic lymphocytic leukemia and small lymphocytic lymphoma represents concerning drug approval patterns in the United States and a weakness in evidence generation.     

The role of exosomes in metastasis and progression of melanoma

The mechanisms of melanoma metastasis have been the subject of extensive research for decades. Improved diagnostic and therapeutic strategies are of increasing importance for the treatment of melanoma due to its high burden of mortality in the advanced stages of the disease. Intercellular communication is a critical event for the progression of cancer. Collective evidence suggests that exosomes, small extracellular membrane vesicles released by the cells, are important facilitators of intercellular communication between the cells and the surrounding environment. Although the emerging field of exosomes is rapidly gaining traction in the scientific community, there is limited knowledge regarding the role of exosomes in melanoma. This review discusses the multifaceted role of melanoma-derived exosomes in promoting the process of metastasis by modulating the invasive and angiogenic capacity of malignant cells. The future implications of exosome research and the therapeutic potential of exosomes are also discussed.     

基于二氧化硅纳米粒子的抗肿瘤药物递送系统研究进展CSCD

近年来癌症治疗受到广泛关注,二氧化硅纳米颗粒因其独特的理化性质在肿瘤诊疗领域展现巨大潜力。基于二氧化硅纳米粒子的药物输送系统可被动或主动靶向肿瘤组织,并通过刺激响应的方式实现药物在肿瘤部位的可控释放,有效提高抗肿瘤药物在肿瘤部位的浓度,提高治疗效率。同时,二氧化硅纳米粒子通过负载造影剂可实现生物成像功能,用于肿瘤组织定位及药物追踪,实现更高效的抗肿瘤治疗。本文介绍了二氧化硅纳米粒子的制备方式,并对二氧化硅纳米粒子在药物靶向递送系统及生物成像领域中的研究进展进行综述。