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find Keyword "靶向治疗" 90 results
  • 癫痫发作诱导 Wnt/β-连环蛋白信号通路的变化—新型抗癫痫治疗的潜在靶点

    癫痫是临床上最常见的神经系统疾病之一,目前癫痫最常用、最重要的治疗手段仍是药物治疗,而耐药性癫痫的存在成为当前抗癫痫治疗的一大难题。现已证明,Wnt/β-连环蛋白通路,作为大脑神经元发生的分子机制,在癫痫的急性期和慢性形成阶段均发生紊乱。Wnt/β-连环蛋白信号通路参与调节许多癫痫发作诱导的脑内变化,包括神经发生和死亡,从而参与癫痫发作的进展。然而该通路影响神经发生的动态变化及通过靶向干预达到治疗目的的具体作用时间仍需进一步研究。总之,Wnt/β-连环蛋白信号通路紊乱,可能成为未来有前景的抗癫痫靶点。

    Release date:2019-07-15 02:48 Export PDF Favorites Scan
  • Research progress on KRAS mutation in pancreatic tumorigenesis and pancreatic cancer therapy

    ObjectiveTo summarize the research progress of KRAS mutation in pancreatic tumorigenesis and therapy.MethodThe research progress of KRAS mutation in pancreatic tumorigenesis and therapy were summarized by reading the domestic and international literatures published in recent years.ResultsPancreatic cancer had the title of " king of cancer”. More than 90% of pancreatic cancer patients had KRAS mutation. KRAS had a complex relationship with pancreatic cancer through downstream signaling pathways, including Raf (rapidly accelerated fibrosarcoma)-mitogen-activated protein kinase kinase (MEK)-extracellular signal-regulated kinase (ERK), phosphatidylinositol-4, 5-bisphosphate 3-kinase (PI3K)-protein kinase B (AKT), and RalGDS-Ral. Although basic research on pancreatic cancer was deepening, there was still a lack of effective molecular targeted drugs.ConclusionsKRASgene plays an important role in the occurrence of pancreatic cancer. The treatment associated with KRAS mutation provides a more effective prognostic possibility for pancreatic cancer patients.

    Release date:2019-06-05 04:24 Export PDF Favorites Scan
  • 2023美国癫痫学会年会荟萃报道(一)

    美国癫痫学会(American Epilepsy Society,AES)年会是每年一度国际癫痫学界及工业界最受关注的会议。本年度的AES年会自2023年12月1日在奥兰多召开,为期5天,讨论了目前最受关注的癫痫学术领域及重点突破。本系列文章将分为五期,分别对大会每日的精彩内容进行荟萃报道:本文对大会第一日学术议程的内容进行了整理汇总,重点内容包括癫痫及癫痫持续状态药物治疗进展,癫痫认知相关共病,额叶癫痫,癫痫靶向治疗等。

    Release date:2024-03-07 01:49 Export PDF Favorites Scan
  • 葡萄膜黑色素瘤抗血管生成靶向治疗的研究进展

    放射治疗、手术切除、经瞳孔温热疗法、巩膜敷贴治疗、化学药物治疗、免疫治疗等单独或联合应用对改善葡萄膜黑色素瘤(UM)患者生存率无明显差异。抗血管内皮生长因子(VEGF)抑制剂等抗血管生成靶向治疗与化学药物治疗、放射治疗等联合应用可明显提高疗效。但单独使用抗VEGF治疗UM效果并不理想, 而且还存在VEGF抑制剂导致肿瘤形成和转移播散的风险。虽然UM的抗血管生成靶向治疗取得了一些进展, 但是离真正的临床应用还有相当长的距离。需要进一步加强对UM的发病机制研究, 特别是UM新生血管发生发展机制方面的研究, 探索可能的干预靶点; 同时加强UM的转化医学研究, 筛选靶向治疗UM的新药物、新方法。

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  • Lenvatinib in the treatment of locally advanced thyroid cancer: a single-center prospective clinical study

    ObjectiveTo evaluate the safety and efficacy of lenvatinib as targeted therapy for locally advanced thyroid cancer. MethodsThe data of 17 patients with locally advanced thyroid cancer who received targeted therapy in the Department of Head and Neck Surgery, Clinical Oncology School of Fujian Cancer Hospital from September 2021 to June 2023 were prospectively collected and analyzed. ResultsSeventeen patients received lenvatinib for a median of 8 weeks (4–32 weeks), 5 patients achieved partial response, 11 patients achieved stable disease, and 1 patient experienced progressive disease. The objective response and disease control rates were 29.4% (5/17) and 94.1% (16/17) respectively, the median tumor diameter of the target lesion decreased from 43 mm before treatment to 12 mm after treatment. Five patients did not undergo surgery because of tumor progression and their refusal; R0/1 resection was achieved in 11 of the 12 remaining patients (91.7%). All patients suffered from drug-related adverse events, and the commonest drug-related adverse events were hypertension (7/17, 41.2%), diarrhea (6/17, 35.3%), and proteinuria (5/17, 29.4%). There were no major drug-related adverse events. ConclusionPreliminary analysis indicates that lenvatinib is effective and safe for targeted therapy of locally advanced thyroid cancer, with a relatively high rate of R0/1 resection.

    Release date:2024-11-27 03:04 Export PDF Favorites Scan
  • Research status and prospect of circular RNAs in diabetic retinopathy

    The mechanisms behind diabetic retinopathy (DR) can be ascribed primarily to retinal microvascular abnormalities, excessive inflammatory response and neurodegeneration. Circular RNA (circRNA) is a type of endogenous non-coding RNA with a special circular structure, which is mainly composed of precursor RNA after shearing and processing. It is widely present in the retina and participates in the occurrence and development of various fundus diseases. CircRNAs express in an abnormal way in retina, serving as “the sponge” for miRNA so as to play roles in dysfunction of retinal vascular, inflammatory response and neurodegeneration in the development of DR. Further studies for circRNAs in DR will illustrate pathophysiology of DR more deeply, shedding light on circRNAs becoming novel biomarkers and molecular targets for diagnosis and treatment, thus achieving the goal of early diagnosis and precise therapy of DR.

    Release date:2022-02-17 02:00 Export PDF Favorites Scan
  • Research progress of HtrA serine peptidase 2 in malignant tumors

    HtrA serine peptidase 2 (HTRA2) is a serine protease existing in the mitochondrial gap. Among the four members of the human HtrA serine peptidase family, HTRA2 is the only protease with clear localization in the cell. It plays a dual role in the maintenance of mitochondrial homeostasis and the promotion of cell apoptosis. HTRA2 has been found to be associated with a variety of tumors. Meanwhile, the expression of HTRA2 can enhance the sensitivity of chemotherapy and radiotherapy, and can be used as a diagnostic and prognostic marker for malignant tumors and a target for combined therapy. This article reviews the structure, biological function and role of HTRA2 in malignant tumors, in order to provide clues and basis for early diagnosis and individualized treatment of tumor patients.

    Release date:2024-02-29 12:02 Export PDF Favorites Scan
  • 表观遗传学调控分子突变在髓系肿瘤中的作用

    基因组研究已经确定在髓系肿瘤包括急性髓系白血病(AML)、骨髓增殖性肿瘤(MPN)和骨髓增生异常综合征(MDS)中,存在多种基因突变,包括DNA甲基转移酶3A、TET甲基胞嘧啶双加氧酶2、异柠檬酸脱氢酶1/2、果蝇zeste基因增强子同源物2和additional sex combs-like 1等,这些表观遗传调控基因突变的发现为髓系肿瘤的研究提供了重要的分子标志和潜在的治疗靶点。该文就AML、MPN和MDS中常见的表观遗传调控基因突变进行综述。

    Release date:2016-10-02 04:54 Export PDF Favorites Scan
  • Progress of Downstaging Therapy in Treating Hepatocellular Carcinoma

    ObjectiveTo summary the progress and status of downstaging therapy in treating hepatocellular carcinoma. MethodsThe related literatures were reviewed and analyzed by searching PubMed and MEDLINE. ResultsAlthough the clinical prognosis of advanced hepatocellular carcinoma was poor, the liver resection or liver transplantation after downstaging therapy could significantly improve the prognosis of patients. However, differences were existed if different downstaging therapies and selections of standard were used. ConclusionTo improve the prognosis of patients with advanced hepatocellular carcinoma, the downstaging therapy should be ingeniously selected based on the situation of the patients.

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  • Regulation study of ubiquitin-specific protease 39 for cell proliferation and apoptosis in colorectal cancer cells

    ObjectiveThis study is aimed to determine the expression of ubiquitin-specific peptidase 39 (USP39) protein in the colorectal cancer (CRC) tissues, and the effect of silencing USP39 gene on the cell growth and cell cycle distribution of CRC cells.Methods① The expressions of USP39 protein in CRC tissues and its paracancerous tissues were determined by immunohistochemical staining method. ② By lentiviral infection, Lv-shUSP39 (KD-1 and KD-2 group) and Lv-shCon (shCon group) were transferred into SW1116 and HCT116 cells, and cells of blank control group did not received any treatment (Con group). To determine the role of USP39 gene in cell growth, MTT assay was performed to draw growth curve, and cell cycle distribution of CRC cells in the 4 groups were determined by flow cytometer.Results① The expression of USP39 protein was higher in CRC tissues compared to adjacent tissues (P=0.007). ② For SW1116 and HCT116 cells, the cell proliferation ability of KD-1 and KD-2 groups were remarkably decreased than those in corresponding shCon and Con groups on 3, 4, and 5-day (P<0.05). ③ Flow cytometry assay showed that, the percentage of G0/G1 phase cells were decreased obviously (P<0.05), while increased significantly in percentage of G2/M phase and number of sub-G1 phase cells in KD-1 group compared with that in the Con group and shCon group of SW1116 and HCT116 cells (P<0.05).ConclusionsThe expression of USP39 protein is highly expressed in CRC tissues. Knockdowning of USP39 gene can inhibit cell proliferation and promote cell apoptosis.

    Release date:2018-12-13 02:01 Export PDF Favorites Scan
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