Fu, fluorouracil

Fu,氟尿嘧啶
  • 文章类型: Journal Article
    UNASSIGNED: Colorectal cancers are the second most common cancers overall and are the third deadliest cancers. Complete resection is the treatment of choice for rectal cancers and chemoradiotherapy (CRT) is strongly recommended in stage 2 and 3. Low anterior resection (LAR) is the most common procedure used, but it requires the use of stapler which might be very expensive as one study estimated the median cost of LAR inpatients to be over 13.000 USD. However, coloanal pull-through (PT) used to be the common procedure before introducing staplers in the twentieth century and can be less expensive, but with higher complication rates.
    UNASSIGNED: This is a retrospective case-control study from patients\' records who underwent either LAR or PT for their rectal cancer in Syria. All patients had either stage 2 or 3 cancer and were treated by the same group of surgeons and received the same adjuvant and neoadjuvant CRT protocol. Patients from both groups had the same prognosis and stages.
    UNASSIGNED: This study included 60 participants, of which, 30 had LAR and 30 had PT. They all had successful removal of the cancer and follow-ups were for 1 year after the surgery. There were no significant differences between the two procedures in post-operative leak, urinary retention, stricture, sexual function and recurrence (p > 0.05). However, post-operative incontinence was more frequent with PT (p = 0.027).
    UNASSIGNED: PT can be an acceptable substitute of LAR in low income settings despite having higher incidence of incontinence.
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  • 文章类型: Journal Article
    乳腺癌是环境因素和遗传因素之间多种相互作用的结果。传统上,根据组织病理学和临床特征治疗乳腺癌。像人类基因组微阵列这样的DNA技术现在已经部分整合到临床实践中,并用于开发新的“个性化药物”和“药物遗传学”,以提高癌症药物的效率和安全性。我们研究了四种已建立的治疗方法-ER导管乳腺癌-对差异基因表达的影响。治疗包括单药他莫昔芬,两剂多西他赛和卡培他滨,或联合三剂CAF(环磷酰胺,阿霉素,和氟尿嘧啶)和CMF(环磷酰胺,甲氨蝶呤,和氟尿嘧啶)。Genevestigator8.1.0用于比较浸润性导管癌患者的五个数据集,未经治疗或用选定的药物治疗,来自健康控制的人。我们确定了74个差异表达基因涉及三个途径,即,凋亡(外在和内在),氧化信号,和PI3K/Akt信令。处理影响了凋亡基因的表达(TNFRSF10B[TRAIL],FAS,CASS3/6/7/8,PMAIP1[NOXA],BNIP3L,BNIP3、BCL2A1和BCL2),氧化应激相关基因(NOX4,XDH,MAOA,GSR,GPX3和SOD3),和PI3K/Akt通路基因(ERBB2[HER2])。乳腺癌治疗是复杂的,患者的药物反应和疗效各不相同。这就需要确定新的生物标志物来预测药物反应。利用现有数据和新技术。GSR,NOX4、CASP3和ERBB2是预测原发性ER+导管乳腺癌治疗反应的潜在生物标志物。
    Breast cancer arises as a result of multiple interactions between environmental and genetic factors. Conventionally, breast cancer is treated based on histopathological and clinical features. DNA technologies like the human genome microarray are now partially integrated into clinical practice and are used for developing new \"personalized medicines\" and \"pharmacogenetics\" for improving the efficiency and safety of cancer medications. We investigated the effects of four established therapies-for ER+ ductal breast cancer-on the differential gene expression. The therapies included single agent tamoxifen, two-agent docetaxel and capecitabine, or combined three-agents CAF (cyclophosphamide, doxorubicin, and fluorouracil) and CMF (cyclophosphamide, methotrexate, and fluorouracil). Genevestigator 8.1.0 was used to compare five datasets from patients with infiltrating ductal carcinoma, untreated or treated with selected drugs, to those from the healthy control. We identified 74 differentially expressed genes involved in three pathways, i.e., apoptosis (extrinsic and intrinsic), oxidative signaling, and PI3K/Akt signaling. The treatments affected the expression of apoptotic genes (TNFRSF10B [TRAIL], FAS, CASP3/6/7/8, PMAIP1 [NOXA], BNIP3L, BNIP3, BCL2A1, and BCL2), the oxidative stress-related genes (NOX4, XDH, MAOA, GSR, GPX3, and SOD3), and the PI3K/Akt pathway gene (ERBB2 [HER2]). Breast cancer treatments are complex with varying drug responses and efficacy among patients. This necessitates identifying novel biomarkers for predicting the drug response, using available data and new technologies. GSR, NOX4, CASP3, and ERBB2 are potential biomarkers for predicting the treatment response in primary ER+ ductal breast carcinoma.
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  • 文章类型: Case Reports
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  • 文章类型: Journal Article
    小梁切除术是青光眼外科治疗的主要手段,而由于术后滤过泡的疤痕,成功率并不令人满意。预防瘢痕的临床对策是术中干预或重复结膜下注射。在这里,我们设计了一种能够转运氟尿嘧啶和抗TGF-β2寡核苷酸的共递送系统,通过局部滴注协同抑制成纤维细胞增殖.这种共递送系统是基于阳离子树枝状聚合物核心(PAMAM)构建的,将氟尿嘧啶包裹在疏水腔内,并与表面氨基缩合寡核苷酸,并进一步用透明质酸和细胞穿透肽进行修饰。共递送系统自组装成纳米级复合物,具有增加的细胞摄取,并且能够有效抑制成纤维细胞的增殖。兔小梁切除术模型的体内研究进一步证实了复合物的抗纤维化功效,延长了过滤泡的存活时间,并在伤口愈合过程中保持了其高度和程度,与术中使用氟尿嘧啶浸润相比,对瘢痕预防具有同等效果。通过免疫组织化学染色的定性观察和通过Western印迹的定量分析都表明TGF-β2表达被共递送复合物抑制。我们的研究提供了一种潜在的方法,有望保证小梁切除术的成功率并延长滤过泡的存活时间。
    Trabeculectomy is the mainstay of surgical glaucoma treatment, while the success rate was unsatisfying due to postoperative scarring of the filtering blebs. Clinical countermeasures for scar prevention are intraoperative intervention or repeated subconjunctival injections. Herein, we designed a co-delivery system capable of transporting fluorouracil and anti-TGF-β2 oligonucleotide to synergistically inhibit fibroblast proliferation via topical instillation. This co-delivery system was built based on a cationic dendrimer core (PAMAM), which encapsulated fluorouracil within hydrophobic cavity and condensed oligonucleotide with surface amino groups, and was further modified with hyaluronic acid and cell-penetrating peptide penetratin. The co-delivery system was self-assembled into nanoscale complexes with increased cellular uptake and enabled efficient inhibition on proliferation of fibroblast cells. In vivo studies on rabbit trabeculectomy models further confirmed the anti-fibrosis efficiency of the complexes, which prolonged survival time of filtering blebs and maintained their height and extent during wound healing process, exhibiting an equivalent effect on scar prevention compared to intraoperative infiltration with fluorouracil. Qualitative observation by immunohistochemistry staining and quantitative analysis by Western blotting both suggested that TGF-β2 expression was inhibited by the co-delivery complexes. Our study provided a potential approach promising to guarantee success rate of trabeculectomy and prolong survival time of filtering blebs.
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  • 文章类型: Case Reports
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