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Statement of Retraction: Protective effect of vasostatin-1 plasmid-like nanoparticles on aortic aneurysm and its mechanism. 撤回声明：类质粒血管生长因子-1对主动脉瘤的保护作用及其机制
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299573
{"title":"Statement of Retraction: Protective effect of vasostatin-1 plasmid-like nanoparticles on aortic aneurysm and its mechanism.","authors":"","doi":"10.1080/21655979.2024.2299573","DOIUrl":"10.1080/21655979.2024.2299573","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2299573"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633117/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139904968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Statement of Retraction: The protective effects of Olmesartan against interleukin-29 (IL-29)-induced type 2 collagen degradation in human chondrocytes. 撤回声明：奥美沙坦对白细胞介素-29（IL-29）诱导的人类软骨细胞 2 型胶原降解的保护作用。
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299551
{"title":"Statement of Retraction: The protective effects of Olmesartan against interleukin-29 (IL-29)-induced type 2 collagen degradation in human chondrocytes.","authors":"","doi":"10.1080/21655979.2024.2299551","DOIUrl":"10.1080/21655979.2024.2299551","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2299551"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633164/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139904975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Statement of Retraction: Functional analysis of ceRNA network of lncRNA TSIX/miR-34a-5p/RBP2 in acute myocardial infarction based on GEO database. 撤回声明：基于GEO数据库的急性心肌梗死中lncRNA TSIX/miR-34a-5p/RBP2的ceRNA网络功能分析
IF 4.9 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-02-01 DOI: 10.1080/21655979.2024.2302657
{"title":"Statement of Retraction: Functional analysis of ceRNA network of lncRNA TSIX/miR-34a-5p/RBP2 in acute myocardial infarction based on GEO database.","authors":"","doi":"10.1080/21655979.2024.2302657","DOIUrl":"10.1080/21655979.2024.2302657","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2302657"},"PeriodicalIF":4.9,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10841004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139650261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Statement of Retraction: miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2. 撤稿声明：miR-148-3p 通过靶向 Bcl2 抑制胃癌细胞的恶性表型和化疗耐药性。
IF 4.9 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-02-01 DOI: 10.1080/21655979.2024.2302654
{"title":"Statement of Retraction: miR-148-3p inhibits gastric cancer cell malignant phenotypes and chemotherapy resistance by targeting Bcl2.","authors":"","doi":"10.1080/21655979.2024.2302654","DOIUrl":"10.1080/21655979.2024.2302654","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2302654"},"PeriodicalIF":4.9,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10841001/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139650262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Isolation of three different sizes of exosomes in an Asian population with different retinal diseases before and after treatment: preliminary results. 在治疗前后患有不同视网膜疾病的亚洲人群中分离出三种不同大小的外泌体：初步结果。
IF 4.9 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2023-12-28 DOI: 10.1080/21655979.2023.2297320
Sung-Yu Wu, Yu-Chien Hung, Chien-Chih Chou, Connie Chen, Chao-Min Cheng, Chihchen Chen, Jyh-Cheng Liou, Min-Yen Hsu
{"title":"Isolation of three different sizes of exosomes in an Asian population with different retinal diseases before and after treatment: preliminary results.","authors":"Sung-Yu Wu, Yu-Chien Hung, Chien-Chih Chou, Connie Chen, Chao-Min Cheng, Chihchen Chen, Jyh-Cheng Liou, Min-Yen Hsu","doi":"10.1080/21655979.2023.2297320","DOIUrl":"10.1080/21655979.2023.2297320","url":null,"abstract":"<p><p>Exosomes are membranous structures measuring between 40-120 nm that are secreted by various cells of the human body into the body fluid system. Exosomes contain proteins, mRNA, miRNA, and signaling molecules, and physiologically they assist in the intercellular transport of proteins and RNA molecules. In this study, we used an immunoaffinity filter paper platform combined with scanning electron microscopy and microfluidic systems to detect the size of exosomes within the aqueous humor. Eight aqueous humor samples showed three distinct sizes of exosomes that were significantly different on scanning electron microscopy(<i>P</i> < 0.01). We further used nanoparticle tracking analysis to assess the size distribution of exosomes within the aqueous humor. We found significantly different distributions of exosomes between patients with three different ocular diseases and patients with normal cataracts as controls. An obvious peak of exomeres(size around 35 nm)was found in the patients with central retinal vein occlusion and vitreous hemorrhage. Flare-ups of large exosomes(size 90-120 nm)were found in the patients with the inflammatory ocular disease pars planitis. No obvious peaks in exomeres or large exosomes were found in the control group. There was a high association between the distribution of exosomes and the pathogenesis of ocular diseases. After intravitreal anti-vascular endothelial growth factor treatment, the aqueous humor from the patients with neovascular diseases showed a significant reduction in exosomes in nanoparticle tracking analysis. These findings suggest that at least three distinct sizes of exosomes exist in the aqueous humor:(1)exomeres:<35 nm;(2)small exosomes:60-80 nm; and (3)large exosomes:90-120 nm. Different sizes of exosomes may have different implications in normal or diseased eyes.</p>","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2297320"},"PeriodicalIF":4.9,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10761085/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139058122","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chimeric antigens displaying GPR65 extracellular loops on a soluble scaffold enabled the discovery of antibodies, which recognized native receptor. 在可溶性支架上显示 GPR65 细胞外环的嵌合抗原使人们发现了能够识别原生受体的抗体。
IF 4.9 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-01-07 DOI: 10.1080/21655979.2023.2299522
Janine Barrett, Seppe Leysen, Cécile Galmiche, Hussein Al-Mossawi, Paul Bowness, Thomas E Edwards, Alastair D G Lawson
{"title":"Chimeric antigens displaying GPR65 extracellular loops on a soluble scaffold enabled the discovery of antibodies, which recognized native receptor.","authors":"Janine Barrett, Seppe Leysen, Cécile Galmiche, Hussein Al-Mossawi, Paul Bowness, Thomas E Edwards, Alastair D G Lawson","doi":"10.1080/21655979.2023.2299522","DOIUrl":"10.1080/21655979.2023.2299522","url":null,"abstract":"<p><p>GPR65 is a proton-sensing G-protein coupled receptor associated with multiple immune-mediated inflammatory diseases, whose function is relatively poorly understood. With few reagents commercially available to probe the biology of receptor, generation of an anti-GPR65 monoclonal antibody was desired. Using soluble chimeric scaffolds, such as ApoE3, displaying the extracellular loops of GPR65, together with established phage display technology, native GPR65 loop-specific antibodies were identified. Phage-derived loop-binding antibodies recognized the wild-type native receptor to which they had not previously been exposed, generating confidence in the use of chimeric soluble proteins to act as efficient surrogates for membrane protein extracellular loop antigens. This technique provides promise for the rational design of chimeric antigens in facilitating the discovery of specific antibodies to GPCRs.</p>","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2299522"},"PeriodicalIF":4.9,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10773626/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139377174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retracted article: MicroRNA-4521 targets hepatoma up-regulated protein (HURP) to inhibit the malignant progression of breast cancer. 被撤回的文章：MicroRNA-4521靶向肝癌上调蛋白（HURP）抑制乳腺癌的恶性进展
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2021-10-26 DOI: 10.1080/21655979.2021.1996016
Changwen Li, Sen Peng, Chuangang Tang
{"title":"Retracted article: MicroRNA-4521 targets hepatoma up-regulated protein (HURP) to inhibit the malignant progression of breast cancer.","authors":"Changwen Li, Sen Peng, Chuangang Tang","doi":"10.1080/21655979.2021.1996016","DOIUrl":"10.1080/21655979.2021.1996016","url":null,"abstract":"<p><p>Changwen Li, Sen Pengb, and Chuangang Tanga. MicroRNA-4521 targets hepatoma up-regulated protein (HURP) to inhibit the malignant progression of breast cancer. Bioengineered. 2021 Oct. doi: 10.1080/21655979.2021.1996016.Since publication, significant concerns have been raised about the compliance with ethical policies for human research and the integrity of the data reported in the article.When approached for an explanation, the authors provided some original data but were not able to provide all the necessary supporting information. As verifying the validity of published work is core to the scholarly record's integrity, we are retracting the article. All authors listed in this publication have been informed.We have been informed in our decision-making by our editorial policies and the COPE guidelines.The retracted article will remain online to maintain the scholarly record, but it will be digitally watermarked on each page as 'Retracted.'</p>","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":" ","pages":"1996016"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10826620/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39562055","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Publisher's Note. 出版商的注意。
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-03-01 DOI: 10.1080/21655979.2024.2326372
{"title":"Publisher's Note.","authors":"","doi":"10.1080/21655979.2024.2326372","DOIUrl":"10.1080/21655979.2024.2326372","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2326372"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10939162/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142799342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Statement of Retraction: The myocardial infarction-associated transcript 2 inhibits lipid accumulation and promotes cholesterol efflux in oxidized low-density lipoprotein-induced THP-1-derived macrophages via inhibiting mitogen-activated protein kinase signaling and activating the nuclear factor erythroid-related factor 2 signaling pathway. 撤回声明：心肌梗死相关转录物2通过抑制丝裂原激活的蛋白激酶信号通路和激活核因子红细胞相关因子2信号通路，抑制氧化低密度脂蛋白诱导的thp -1来源的巨噬细胞的脂质积累，促进胆固醇外流。
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-12-09 DOI: 10.1080/21655979.2024.2299530
{"title":"Statement of Retraction: The myocardial infarction-associated transcript 2 inhibits lipid accumulation and promotes cholesterol efflux in oxidized low-density lipoprotein-induced THP-1-derived macrophages via inhibiting mitogen-activated protein kinase signaling and activating the nuclear factor erythroid-related factor 2 signaling pathway.","authors":"","doi":"10.1080/21655979.2024.2299530","DOIUrl":"10.1080/21655979.2024.2299530","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2299530"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633149/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142799347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Statement of Retraction: Dihydroartemisinin targets fibroblast growth factor receptor 1 (FGFR1) to inhibit interleukin 17A (IL-17A)-induced hyperproliferation and inflammation of keratinocytes. 撤回声明：双氢青蒿素以成纤维细胞生长因子受体1（FGFR1）为靶点，抑制白细胞介素17A（IL-17A）诱导的角朊细胞过度增殖和炎症。
IF 4.2 4区 生物学
Bioengineered Pub Date : 2024-12-01 Epub Date: 2024-02-20 DOI: 10.1080/21655979.2024.2299613
{"title":"Statement of Retraction: Dihydroartemisinin targets fibroblast growth factor receptor 1 (FGFR1) to inhibit interleukin 17A (IL-17A)-induced hyperproliferation and inflammation of keratinocytes.","authors":"","doi":"10.1080/21655979.2024.2299613","DOIUrl":"10.1080/21655979.2024.2299613","url":null,"abstract":"","PeriodicalId":8919,"journal":{"name":"Bioengineered","volume":"15 1","pages":"2299613"},"PeriodicalIF":4.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633118/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139904901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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