EXPRESSION OF CONCERN: Intelligent TAT-Coupled Anti-HER2 Immunoliposomes Knock Downed MDR1 to Produce Chemosensitize Phenotype of Multidrug Resistant Carcinoma

IF 4 2区 生物学 Q2 CELL BIOLOGY
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引用次数: 0

Abstract

EXPRESSION OF CONCERN: N. Gholamian Dehkordi, F. Elahian, P. Khosravian, and S. A. Mirzaei, “Intelligent TAT‑Coupled Anti‑HER2 Immunoliposomes Knock Downed MDR1 to Produce Chemosensitize Phenotype of Multidrug Resistant Carcinoma,” Journal of Cellular Physiology 234, no. 11 (2019): 20769–20778, https://doi.org/10.1002/jcp.28683.

This Expression of Concern is for the above article, published online on 18 April 2019 in Wiley Online Library (wileyonlinelibrary.com), and has been published by agreement between the journal Editor-in-Chief, Robert Heath; and Wiley Periodicals LLC. The Expression of Concern has been agreed due to concerns raised by a third party, which identified overlapping Western blot images in Figures 4(c) and 4(d). The authors stated that the figure legend requires correction. However, further review of the article revealed substantial inconsistencies in Section 3.5, Table 1, and Figure 2 regarding the reported size of the nanocarriers. The authors were unable to provide the original raw data of the Western blot images or offer a satisfactory explanation for these issues. The authors plan to further investigate and characterize particle morphology and have reported to the editor that their results should be forthcoming. However, the Editor-in-Chief and the publisher have decided to publish this Expression of Concern to inform readers that questions regarding the reliability of the reported results remain.

关注的表达:智能tat偶联抗her2免疫脂质体敲低MDR1产生多药耐药癌的化疗敏化表型。
关注表达:N. Gholamian Dehkordi, F. Elahian, P. Khosravian, S. A. Mirzaei,“智能TAT偶联抗HER2免疫脂体敲低MDR1产生多药耐药肿瘤的化学敏感表型”,细胞生理学杂志,第234期。11 (2019): 20769-20778, https://doi.org/10.1002/jcp.28683。上述文章已于2019年4月18日在线发表在Wiley在线图书馆(wileyonlinelibrary.com)上,并经期刊主编Robert Heath;和Wiley期刊有限责任公司。由于第三方提出的担忧,我们同意了关注表达,该第三方在图4(c)和4(d)中发现了重叠的Western blot图像。作者指出图例需要更正。然而,对文章的进一步回顾发现,第3.5节、表1和图2中关于纳米载体尺寸的报道存在实质性的不一致。作者无法提供Western blot图像的原始数据,也无法对这些问题给出令人满意的解释。作者计划进一步研究和表征粒子形态,并向编辑报告他们的结果应该即将到来。然而,总编辑和出版商决定发表这一关注表达,以告知读者关于报告结果可靠性的问题仍然存在。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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