术前控制营养状态评分与肝细胞癌肝切除术后预后的研究进展

肝细胞癌(HCC)是最常见的恶性肿瘤之一。尽管在早期诊断和个体化治疗方面取得了进展,但经根治性切除等治疗后,HCC患者的临床预后仍不佳,复发率高。因此,在HCC患者中识别准确可靠的预后标志物是必要的。作为一种新的免疫营养生物标志物,控制营养状态(CONUT)评分已被报道用于预测癌症患者的预后。本文将对术前CONUT评分与HCC肝切除术后预后的研究进展进行综述。     

信息化技术应用于静脉血栓栓塞症护理的研究进展

综述信息化技术在静脉血栓栓塞症护理领域中风险预测、警报接收与上报、抗凝防治管理、医护人员相关继续医学教育、患者疾病预后管理的应用现状，总结其应用阻碍因素，旨在为我国静脉血栓栓塞症护理信息化建设提供参考。     

肾移植女性受者妊娠管理的研究进展

综述妊娠对女性肾移植患者的影响，肾移植术后妊娠的管理（妊娠前风险提示、妊娠前风险评估、妊娠期免疫抑制剂的应用、妊娠期产检及移植肾功能随访、分娩及麻醉方式的选择、产后喂养方式），肾移植术后多胎妊娠受者的现状等。旨在总结近年来国内外对肾移植术后患者妊娠管理的经验，提升移植专科护理人员对术后妊娠群体的关注度，为有妊娠意愿的肾移植术后患者提供支持。     

王檀教授基于虚寒病机辨证治疗间质性肺疾病的临床经验浅析

间质性肺疾病是一组肺部弥漫性疾病,为呼吸系统疑难病,呼吸致残率、死亡率高,发病率逐年提高。目前间质性肺疾病的相关研究很多,至今尚无特效治疗方法,而中医药对于间质性肺疾病的治疗具有极大的优势。本文对王檀教授治疗间质性肺疾病从"痹"论治、病因病机、临床分型,具体针对内因成痹、外因致病及加重等因素灵活加减,辨治用药方面进行全面总结,为临床提供参考。     

SLC12A5 interacts and enhances SOX18 activity to promote bladder urothelial carcinoma progression via upregulating MMP7

Solute carrier family 12 member 5 (SLC12A5) has an oncogenic role in bladder urothelial carcinoma. The present study aimed to characterize the molecular mechanisms of SLC12A5 in bladder urothelial carcinoma pathogenesis. Functional assays identified that in bladder urothelial carcinoma SLC12A5 interacts with and stabilizes SOX18, and then upregulates matrix metalloproteinase 7 (MMP7). In vivo and in vitro assays were performed to confirm the effect of SLC12A5’s interaction with SOX18 on MMP7‐mediated bladder urothelial carcinoma progression. SLC12A5 was upregulated in human bladder tumors, and correlated with the poor survival of patients with bladder urothelial carcinoma tumor invasion and metastasis, promoted by SLC12A5 overexpression. We demonstrated that SLC12A5 interacted with SOX18, and then upregulated MMP7, thus enhancing tumor progression. Importantly, SLC12A5 expression correlated positively with SOX18 and MMP7 expression in bladder urothelial carcinoma. Furthermore, SLC12A5 expression was suppressed by miR‐133a‐3p. Ectopic expression of SLC12A5 partly abolished miR‐133a‐3p‐mediated suppression of cell migration. SLC12A5‐SOX18 complex‐mediated upregulation on MMP7 was important in bladder urothelial carcinoma progression. The miR‐133a‐3p/SLC12A5/SOX18/MMP7 signaling axis was critical for progression, and provided an effective therapeutic approach against bladder urothelial carcinoma.