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RETRACTION: Long Noncoding RNA HOTTIP Alleviates Oxygen-Glucose Deprivation-Induced Neuronal Injury via Modulating MiR-143/Hexokinase 2 Pathway 回归:长非编码 RNA HOTTIP 通过调节 MiR-143/Hexokinase 2 通路缓解氧-葡萄糖剥夺诱导的神经元损伤
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-25 DOI: 10.1002/jcb.70020

RETRACTION: Y. Wang, G. Li, L. Zhao, and J. Lv, “Long Noncoding RNA HOTTIP Alleviates Oxygen-Glucose Deprivation-Induced Neuronal Injury via Modulating MiR-143/Hexokinase 2 Pathway,” Journal of Cellular Biochemistry 119, no. 12 (2018): 10107-10117, https://doi.org/10.1002/jcb.27348.

The above article, published online on 20 August 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Multiple image elements within Figure 2 C were found to have been published previously by different authors in different scientific contexts. The authors were invited to comment on these concerns but did not respond. Accordingly, the article is retracted as the editors have lost confidence in the integrity and reliability of the full body of data presented in the article and consider its conclusions invalid. The authors were informed of the retraction.

引用本文:王艳,李国光,赵亮,吕军,“长链非编码RNA HOTTIP通过调控MiR-143/己糖激酶2通路减轻氧葡萄糖剥夺诱导的神经元损伤”,《细胞生物化学》,第11期。12 (2018): 10107-10117, https://doi.org/10.1002/jcb.27348.The上述文章于2018年8月20日在线发表在Wiley online Library (wileyonlinelibrary.com)上,经主编Christian Behl同意撤回;和Wiley期刊有限责任公司。由于第三方提出的担忧,已同意撤回。图2c中的多个图像元素被发现已经由不同的作者在不同的科学背景下发表过。作者被邀请对这些担忧发表评论,但没有回应。因此,由于编辑对文章中提供的全部数据的完整性和可靠性失去信心,并认为其结论无效,因此文章被撤回。作者被告知撤稿。
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引用次数: 0
RETRACTION: Crocin Synergistically Enhances the Antiproliferative Activity of 5-Flurouracil Through Wnt/PI3K Pathway in a Mouse Model of Colitis-Associated Colorectal Cancer 在结肠炎相关结直肠癌小鼠模型中,藏红花素通过Wnt/PI3K途径协同增强5-氟尿嘧啶的抗增殖活性
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-23 DOI: 10.1002/jcb.70015

RETRACTION: F. Amerizadeh, N. Rezaei, F. Rahmani, S. M. Hassanian, R. Moradi-Marjaneh, H. Fiuji, N. Boroumand, A. Nosrati-Tirkani, M. Ghayour-Mobarhan, G. A. Ferns, M. Khazaei, and A. Avan, “Crocin Synergistically Enhances the Antiproliferative Activity of 5-Flurouracil Through Wnt/PI3K Pathway in a Mouse Model of Colitis-Associated Colorectal Cancer,” Journal of Cellular Biochemistry 119, no. 12 (2018): 10250-10261, https://doi.org/10.1002/jcb.27367.

The above article, published online on August 20, 2018, in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl, and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Figure 6B was found to contain inappropriate splicing sites and methodological flaws. Additionally, in Figure 5A and 5a, no correlation was observed between samples at low and high magnification. The authors did not provide clarification on these issues or the original data. Accordingly, the article is retracted as the editors have lost confidence in the integrity and accuracy of the whole body of data presented in the article and consider its conclusions invalid. The authors have been informed of the decision of retraction.

引用本文:F. Amerizadeh, N. Rezaei, F. Rahmani, S. M. Hassanian, R. moradii - marjaneh, H. Fiuji, N. Boroumand, a . nosratii - tirkani, M. ghaour - mobarhan, G. a . Ferns, M. Khazaei, a . Avan,“藏红花素通过Wnt/PI3K途径协同增强5-尿嘧啶在结肠炎相关结直肠癌模型中的抗增殖活性”,细胞生物化学杂志,第119期。12 (2018): 10250-10261, https://doi.org/10.1002/jcb.27367.The上述文章于2018年8月20日在线发表在Wiley在线图书馆(wileyonlinelibrary.com)上,经期刊主编Christian Behl和Wiley期刊有限责任公司同意撤回。由于第三方提出的担忧,已同意撤回。发现图6B包含不合适的剪接位点和方法缺陷。此外,在图5A和5A中,在低倍率和高倍率下,样品之间没有相关性。作者没有对这些问题或原始数据提供澄清。因此,由于编辑对文章中提供的整个数据的完整性和准确性失去信心,并认为其结论无效,因此文章被撤回。作者已被告知撤稿的决定。
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引用次数: 0
RETRACTION: Forkhead Box p3 Controls Progression of Oral Lichen Planus by Regulating MicroRNA-146a 缩回:叉头盒p3通过调控MicroRNA-146a调控口腔扁平苔藓的进展
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-23 DOI: 10.1002/jcb.70019

RETRACTION: J. Wang, L. Yang, L. Wang, Y. Yang, and Y. Wang, “Forkhead Box p3 Controls Progression of Oral Lichen Planus by Regulating MicroRNA-146a, ” Journal of Cellular Biochemistry 119, no. 11 (2018): 8862-8871, https://doi.org/10.1002/jcb.27139.

The above article, published online on 20 August 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Image elements within Figures 2E, 3D and 5 A were found to have been published previously by different authors in different scientific contexts. The authors were invited to comment on these concerns but did not respond. Accordingly, the article is retracted as the editors have lost confidence in the integrity and reliability of the full body of data presented in the article and consider its conclusions invalid. The authors were informed of the retraction.

退稿:J. Wang, L. Yang, L. Wang, Y. Yang, and Y. Wang, "Forkhead Box p3 Controls Progression of Oral Lichen Planus by Regulating MicroRNA-146a, " Journal of Cellular Biochemistry 119, no:8862-8871, https://doi.org/10.1002/jcb.27139.The 上述文章于 2018 年 8 月 20 日在线发表于 Wiley Online Library (wileyonlinelibrary.com),经期刊主编 Christian Behl 和 Wiley Periodicals LLC 协议,该文章已被撤回。同意撤稿的原因是第三方提出的疑虑。图 2E、3D 和 5 A 中的图像元素被发现曾由不同作者在不同科学背景下发表过。我们邀请作者就这些问题发表评论,但他们没有回应。因此,由于编者对文章中提供的全部数据的完整性和可靠性失去信心,并认为其结论无效,文章被撤回。已将撤稿通知作者。
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引用次数: 0
Deficiency of HSF4 Increases the Secretion of Small Extracellular Vesicles via Upregulation of Chaperone-Mediated Autophagy 缺乏HSF4通过上调伴侣介导的自噬增加细胞外小泡的分泌
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-10 DOI: 10.1002/jcb.70031
Jingjing Liu, Xuhui Liu, Xiaohang Xie, Wei Si, Yuhang Zhang, Mengjiao Xue, Xuyan Peng, Mingjun Jiang, Shanshan Du, Jingzhi Shao, Yi Mao, Fengyan Zhang, Yanzhong Hu

Small extracellular vesicles (SEVs) are membrane-bound vesicles secreted by cells that facilitate intercellular communication. This study reveals how heat shock transcription factor 4 (HSF4) deficiency regulates SEV secretion in lens epithelial cells through chaperone-mediated autophagy (CMA). Compared to mLEC/HA-Hsf4b cells, SEVs secreted by HSF4-deficient mLEC/Hsf4−/− cells showed significantly increased levels of CMA-related proteins (HSP70, HSC70, LAMP2A, and HSP90) and EGFR, while LC3 II levels were reduced. Additionally, EGFR-enriched SEVs activated downstream ERK/AKT signaling pathways, promoting the proliferation and migration of lens epithelial cells and inducing epithelial–mesenchymal transition (EMT). Further inhibition experiments showed that blocking HSP70 and HSP90 with apoptozole and retaspimycin, or silencing LAMP2A with siRNA, reduced SEV secretion in HSF4-deficient cells. Collectively, enhanced CMA activity and increased SEV secretion induced by HSF4 deficiency may represent a potential mechanism underlying congenital cataract development.

小细胞外囊泡(sev)是由细胞分泌的膜结合囊泡,促进细胞间的通讯。本研究揭示了热休克转录因子4 (HSF4)缺乏如何通过伴侣介导的自噬(CMA)调节晶状体上皮细胞的SEV分泌。与mLEC/HA-Hsf4b细胞相比,Hsf4缺陷mLEC/Hsf4−/−细胞分泌的sev显示cma相关蛋白(HSP70、HSC70、LAMP2A和HSP90)和EGFR水平显著升高,而LC3 II水平降低。此外,富含egfr的sev激活下游ERK/AKT信号通路,促进晶状体上皮细胞的增殖和迁移,诱导上皮-间质转化(EMT)。进一步的抑制实验表明,用凋亡唑和再阿霉素阻断HSP70和HSP90,或用siRNA沉默LAMP2A,可减少hsf4缺陷细胞中SEV的分泌。综上所述,HSF4缺乏引起的CMA活性增强和SEV分泌增加可能是先天性白内障发展的潜在机制。
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引用次数: 0
Molecular Structure Insights Into Antioxidant, Anti-Inflammatory, and Computational Investigations: Molecular Docking and Dynamics Studies on Enzyme Inhibitors 分子结构洞察抗氧化,抗炎和计算研究:酶抑制剂的分子对接和动力学研究
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-08 DOI: 10.1002/jcb.70033
Ismail sheriff Parvin, Hamza Serina Banu, Ekambaram Gayathiri, Palanisamy Prakash, Somdatta Y. Chaudhari, Thangaraj Pratheep, Subramanian Deepika Priyadharshini, Muthiah Pugalenthi, Jayapandian Narmathasri

Solanum erianthum D. Don (Solanaceae) species has wide range of usage in treating disease in folk medicine. This study focused on the isolation and characterization of Phytol, βCaryophyllene (βc), and Methoxy - 4- Quercetin (M4Q) from Solanum erianthum leaf and seed fractions. These three compounds were studied for antioxidant activities using DPPH, SOD, and FRAP assays, accompanied by molecular docking, molecular dynamics, and ADMET tools. Our results showed that, Methoxy 4-Quercetin scored good antioxidant potential in the studied assays, with a stable conformation and favorable properties. Docking analysis was used to determine the binding energies of these compounds with different receptor proteins and ligand complexes, as well as their stability, conformation, and binding energy in molecular dynamics. Pharmacokinetic compounds exhibit kinetic values and drug-like characteristics, indicating their biological activity. Competent studies on the compounds using in silico analyses showed that all compounds have notable anti-cardiotoxic and anti-inflammatory effects. Thus, studies on phytocompounds as effective leads to the improvement of anti-inflammatory and anti-cardio agents are necessary for further in vivo studies.

摘要龙葵属(Solanum erianthum D. Don)在民间医学中具有广泛的治疗疾病的用途。本研究主要从茄子叶片和种子中分离鉴定叶绿醇、β石竹烯(βc)和甲氧基- 4-槲皮素(M4Q)。通过DPPH、SOD和FRAP检测,结合分子对接、分子动力学和ADMET工具,研究了这三种化合物的抗氧化活性。结果表明,甲氧基4-槲皮素具有良好的抗氧化活性,具有稳定的构象和良好的性质。通过对接分析,确定了这些化合物与不同受体蛋白和配体复合物的结合能,以及它们在分子动力学中的稳定性、构象和结合能。药代动力学化合物表现出动力学值和药物样特性,表明其生物活性。对化合物的硅分析研究表明,所有化合物都具有显著的抗心脏毒性和抗炎作用。因此,研究植物化合物作为有效的抗炎和抗心脏药物的改善是进一步的体内研究的必要条件。
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引用次数: 0
RETRACTION: Fibronectin Promotes Cervical Cancer Tumorigenesis Through Activating FAK Signaling Pathway 收缩:纤连蛋白通过激活FAK信号通路促进宫颈癌的发生
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-03 DOI: 10.1002/jcb.70022

RETRACTION: Y. Zhou, C. Shu, and Y. Huang, “Fibronectin Promotes Cervical Cancer Tumorigenesis Through Activating FAK Signaling Pathway,” Journal of Cellular Biochemistry 120, no. 7 (2019): 10988–10997, https://doi.org/10.1002/jcb.28282.

The above article, published online on 11 April 2019 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the authors; the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Multiple image elements in Figures 2B and 3C were found to have been previously published by different author groups in different scientific contexts. Additionally, Figure 3C contains duplication, with the same panel being used to depict different scientific contexts. Accordingly, the article is retracted as the editors consider its conclusions to be invalid.

引用本文:周艳,舒春春,黄艳,“纤维连接蛋白通过激活FAK信号通路促进宫颈癌的发生”,《细胞生物化学杂志》,第12期。7 (2019): 10988-10997, https://doi.org/10.1002/jcb.28282.The上述文章于2019年4月11日在线发表在Wiley在线图书馆(wileyonlinelibrary.com),经作者同意撤回;杂志主编克里斯蒂安·贝尔;和Wiley期刊有限责任公司。由于第三方提出的担忧,已同意撤回。图2B和图3C中的多个图像元素被发现曾由不同的作者团队在不同的科学背景下发表过。此外,图3C包含重复,用相同的面板来描述不同的科学背景。因此,这篇文章被撤回,因为编辑认为其结论无效。
{"title":"RETRACTION: Fibronectin Promotes Cervical Cancer Tumorigenesis Through Activating FAK Signaling Pathway","authors":"","doi":"10.1002/jcb.70022","DOIUrl":"https://doi.org/10.1002/jcb.70022","url":null,"abstract":"<p><b>RETRACTION:</b> Y. Zhou, C. Shu, and Y. Huang, “Fibronectin Promotes Cervical Cancer Tumorigenesis Through Activating FAK Signaling Pathway,” <i>Journal of Cellular Biochemistry</i> 120, no. 7 (2019): 10988–10997, https://doi.org/10.1002/jcb.28282.</p><p>The above article, published online on 11 April 2019 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the authors; the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Multiple image elements in Figures 2B and 3C were found to have been previously published by different author groups in different scientific contexts. Additionally, Figure 3C contains duplication, with the same panel being used to depict different scientific contexts. Accordingly, the article is retracted as the editors consider its conclusions to be invalid.</p>","PeriodicalId":15219,"journal":{"name":"Journal of cellular biochemistry","volume":"126 4","pages":""},"PeriodicalIF":3.0,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcb.70022","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143761849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
RETRACTION: LncRNA SNHG1 Regulates Cerebrovascular Pathologies as a Competing Endogenous RNA Through HIF-1α/VEGF Signaling in Ischemic Stroke 在缺血性卒中中,LncRNA SNHG1作为竞争内源性RNA通过HIF-1α/VEGF信号通路调控脑血管病理
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-03 DOI: 10.1002/jcb.70017

RETRACTION: L. Zhang, X. Luo, F. Chen, W. Yuan, X. Xiao, X. Zhang, Y. Dong, Y. Zhang, and Y. Liu, “LncRNA SNHG1 Regulates Cerebrovascular Pathologies as a Competing Endogenous RNA Through HIF-1α/VEGF Signaling in Ischemic Stroke, ” Journal of Cellular Biochemistry 119, no. 7 (2018): 5460-5472, https://doi.org/10.1002/jcb.26705.

The above article, published online on 27 January 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Image elements within Figures 3 C and 6 F were found to have been published previously by different authors in different scientific contexts. The authors were invited to comment on these concerns but did not respond. Accordingly, the article is retracted as the editors have lost confidence in the integrity and reliability of the full body of data presented in the article and consider its conclusions invalid. The authors were informed of the retraction.

引用本文:张莉,罗晓霞,陈峰,袁伟,肖晓霞,张晓霞,董艳,张艳,刘艳,“LncRNA SNHG1作为竞争内源性RNA通过HIF-1α/VEGF信号通路调控缺血性脑卒中的脑血管病,细胞生物化学119,no。7 (2018): 5460-5472, https://doi.org/10.1002/jcb.26705.The上述文章于2018年1月27日在线发表在Wiley online Library (wileyonlinelibrary.com)上,经主编Christian Behl同意撤回;和Wiley期刊有限责任公司。由于第三方提出的担忧,已同意撤回。图3c和图6f中的图像元素被发现以前由不同的作者在不同的科学背景下发表过。作者被邀请对这些担忧发表评论,但没有回应。因此,由于编辑对文章中提供的全部数据的完整性和可靠性失去信心,并认为其结论无效,因此文章被撤回。作者被告知撤稿。
{"title":"RETRACTION: LncRNA SNHG1 Regulates Cerebrovascular Pathologies as a Competing Endogenous RNA Through HIF-1α/VEGF Signaling in Ischemic Stroke","authors":"","doi":"10.1002/jcb.70017","DOIUrl":"https://doi.org/10.1002/jcb.70017","url":null,"abstract":"<p><b>RETRACTION:</b> L. Zhang, X. Luo, F. Chen, W. Yuan, X. Xiao, X. Zhang, Y. Dong, Y. Zhang, and Y. Liu, “LncRNA SNHG1 Regulates Cerebrovascular Pathologies as a Competing Endogenous RNA Through HIF-1α/VEGF Signaling in Ischemic Stroke, ” <i>Journal of Cellular Biochemistry</i> 119, no. 7 (2018): 5460-5472, https://doi.org/10.1002/jcb.26705.</p><p>The above article, published online on 27 January 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Image elements within Figures 3 C and 6 F were found to have been published previously by different authors in different scientific contexts. The authors were invited to comment on these concerns but did not respond. Accordingly, the article is retracted as the editors have lost confidence in the integrity and reliability of the full body of data presented in the article and consider its conclusions invalid. The authors were informed of the retraction.</p>","PeriodicalId":15219,"journal":{"name":"Journal of cellular biochemistry","volume":"126 4","pages":""},"PeriodicalIF":3.0,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcb.70017","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143761848","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
RETRACTION: Lycopene Protects Keratinocytes Against UVB Radiation-Induced Carcinogenesis via Negative Regulation of FOXO3a Through the mTORC2/AKT Signaling Pathway 摘要:番茄红素通过mTORC2/AKT信号通路负调控FOXO3a,保护角质形成细胞免受UVB辐射诱导的癌变
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-04-03 DOI: 10.1002/jcb.70016

RETRACTION: P. Chen, S. Xu, and J. Qu, “Lycopene Protects Keratinocytes Against UVB Radiation-Induced Carcinogenesis via Negative Regulation of FOXO3a Through the mTORC2/AKT Signaling Pathway,” Journal of Cellular Biochemistry 119, no. 1 (2018): 366-377, https://doi.org/10.1002/jcb.26189.

The above article, published online on 6 June 2017 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl; and Wiley Periodicals LLC. The retraction has been agreed due to concerns raised by third parties. Multiple image elements within Figures 2 A and 4 A were found to have been published previously and/or subsequently by different authors in different scientific contexts. Furthermore, evidence of inappropriate image editing/manipulation were found within Figure 3 C. The authors were invited to comment on these concerns but did not respond. Accordingly, the article is retracted as the editors have lost confidence in the integrity and reliability of the full body of data presented in the article and consider its conclusions invalid. The authors were informed of the retraction.

引用本文:陈鹏,徐世生,曲俊,“番茄红素通过mTORC2/AKT信号通路负调控FOXO3a对UVB辐射诱导的角质形成细胞的保护作用”,《细胞生物化学》,第11期。1 (2018): 366-377, https://doi.org/10.1002/jcb.26189.The上述文章于2017年6月6日在Wiley online Library (wileyonlinelibrary.com)上发表,经主编Christian Behl同意撤回;和Wiley期刊有限责任公司。由于第三方提出的担忧,已同意撤回。图2a和图4a中的多个图像元素被发现在之前和/或之后由不同的作者在不同的科学背景下发表。此外,在图3c中发现了不适当的图像编辑/操作的证据。作者被邀请对这些担忧发表评论,但没有回应。因此,由于编辑对文章中提供的全部数据的完整性和可靠性失去信心,并认为其结论无效,因此文章被撤回。作者被告知撤稿。
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引用次数: 0
RETRACTION: Characterization of the Kynurenine Pathway in Skin-Derived Fibroblasts and Keratinocytes 回撤:皮肤源性成纤维细胞和角化细胞中犬尿氨酸通路的表征
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-03-31 DOI: 10.1002/jcb.70013

RETRACTION: D. Sheipouri, R. Grant, S. Bustamante, D. Lovejoy, G. J. Guillemin, and N. Braidy, “Characterization of the Kynurenine Pathway in Skin-Derived Fibroblasts and Keratinocytes,” Journal of Cellular Biochemistry 116, no. 6 (2015): 903-922. https://doi.org/10.1002/jcb.25019.

The above article, published online on January 12, 2015, in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Christian Behl, and Wiley Periodicals LLC. The journal received notice from a third party regarding evidence of duplication and image manipulation between the QPRT and KMO panels in Figure 5D as well as the QPRT and KAT-II panels in Figure 5B. The publisher confirmed these duplications. Some authors responded to an inquiry by the publisher but were not able to provide an explanation for the duplicated panels and were not able to provide original data for verification. An initial investigation by the University of New South Wales Conduct & Integrity Office concluded that the immunochemistry data presented in this article had been misrepresented, fabricated and/or falsified and warranted further investigation by an independent research misconduct inquiry panel. The retraction has been agreed to because the evidence of image duplication and manipulation compromises the integrity of the study and the conclusions presented in the article. S.B. and D.L. agree with the retraction. All other authors did not respond to our notice regarding the retraction.

引用本文:D. Sheipouri, R. Grant, S. Bustamante, D. Lovejoy, G. J. Guillemin, N. Braidy,“皮肤源性成纤维细胞和角质形成细胞中犬尿氨酸途径的表征”,《细胞生物化学杂志》116,第1期。6(2015): 903-922。https://doi.org/10.1002/jcb.25019.The上述文章于2015年1月12日在线发表在Wiley online Library (wileyonlinelibrary.com)上,经期刊主编Christian Behl和Wiley期刊有限责任公司协议,该文章已被撤回。该期刊收到第三方通知,称有证据表明图5D中的QPRT和KMO图以及图5B中的QPRT和KAT-II图之间存在复制和图像操纵。出版商证实了这些重复。一些作者答复了出版商的询问,但无法对重复的面板作出解释,也无法提供原始数据供核查。新南威尔士大学的一项初步调查表明;诚信办公室的结论是,本文中提供的免疫化学数据被歪曲、捏造和/或伪造,有必要由一个独立的研究不端行为调查小组进行进一步调查。由于图像复制和篡改的证据损害了研究的完整性和文章中提出的结论,因此同意撤回。s。b。和d。l。同意撤回。所有其他作者都没有回应我们关于撤稿的通知。
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引用次数: 0
Cross-Kingdom Genomic Conservation of Putative Human Sleep-Related Genes: Phylogenomic Evidence From Chlamydomonas reinhardtii 假定的人类睡眠相关基因的跨界基因组保护:来自莱茵衣藻的系统基因组证据
IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-03-31 DOI: 10.1002/jcb.70030
Seithikurippu R. Pandi-Perumal, Konda Mani Saravanan, Sayan Paul, George C. Abraham, David Warren Spence, Saravana Babu Chidambaram

Sleep is a widespread and evolutionarily conserved process observed in diverse organisms, from jellyfish to mammals, hinting at its origin as a life-supporting mechanism over 500 million years ago. Although its fundamental purpose and mechanisms remain unclear, sleep's evolution and adaptive significance continue to be debated. This study explores the evolutionary origins of sleep using Chlamydomonas reinhardtii as a model organism, identifying 112 putative sleep-related genes across species and highlighting the evolutionary conservation of sleep-regulatory pathways. Additionally, discovering uncharacterized proteins with high sequence similarity and significant e-values suggests unexplored roles in sleep regulation, underscoring the potential of C. reinhardtii to reveal new insights into the molecular basis of sleep. This study provides a foundation for identifying previously unknown sleep-associated proteins, particularly within single-celled organisms, which may offer novel perspectives on the biological role of sleep. The study demonstrates that phylogenomic analysis of diverse model organisms can expand our understanding of the evolutionary trajectory of sleep and its fundamental function, paving the way for further research in sleep biology and its health implications. Overall, the fundamental functions of sleep observed in higher animal phyla originated from its primordial activities, demonstrating an evolutionary continuum wherein more specialized tasks were integrated with sleep's essential restorative properties.

从水母到哺乳动物,睡眠是一种广泛存在的进化保守过程,暗示其起源是5亿多年前的一种生命维持机制。尽管其基本目的和机制尚不清楚,但睡眠的进化和适应意义仍在争论中。本研究以莱茵衣藻(Chlamydomonas reinhardtii)为模式生物,探索了睡眠的进化起源,确定了112个跨物种的睡眠相关基因,并强调了睡眠调节途径的进化保护。此外,发现具有高序列相似性和显著e值的未表征蛋白表明在睡眠调节中未被探索的作用,强调了C. reinhardtii揭示睡眠分子基础的新见解的潜力。这项研究为识别以前未知的睡眠相关蛋白,特别是单细胞生物中的睡眠相关蛋白提供了基础,这可能为睡眠的生物学作用提供新的视角。该研究表明,多种模式生物的系统基因组分析可以扩展我们对睡眠进化轨迹及其基本功能的理解,为进一步研究睡眠生物学及其健康意义铺平道路。总的来说,在高等动物门中观察到的睡眠的基本功能起源于其原始活动,证明了一个进化连续体,其中更专门的任务与睡眠的基本恢复特性相结合。
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引用次数: 0
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Journal of cellular biochemistry
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