Literature DB >> 19878769

Chapter 1: Introduction.

Saverio Bettuzzi1.   

Abstract

Since the beginning, Clusterin (CLU) was revealed not as simple to study, and certainly not a single protein. The growing research interest on CLU soon produced many contributions by independent laboratories working in different systems. Thus, many different names or acronyms have been given to CLU in the early years after its discovery. Now, a general consensus recommend the name Clusterin and the abbreviation CLU. CLU was first described as a glycoprotein found nearly ubiquitous in tissues and body fluids. This early knowledge is mostly related to the secretory form of CLU (sCLU), which is exported from the cell and released in secretions acting as an extracellular chaperone. But CLU can also enter the nucleus. The detection of nCLU (nuclear CLU), which is usually associated to cell death, is now emerging as a very important event making this issue even more complex. This may explain why CLU is still often described as an "enigmatic" protein. The use of the term "enigmatic" is a clear indication that too many aspects related to the biological function(s) of CLU and its possible role in pathogenesis have been obscure, or very difficult to interpret, for long time. Contradictory findings on CLU are also present in the literature, sometimes due to technical biases or alternative interpretation of the same result. The aim of the book is ambitious: through a careful review of old data, in the light of novel information and up to date methods and hypotheses, we will try to simplify the picture for the reader and bring more light in a field still perceived to be too obscure to fully appreciate its importance and potential implementation in the clinical setting. This introduction will provide a brief general history and a critical view of the discovery of CLU with the aim to underline what is new in the field and what is now obsolete. In the rest of the book, conclusions and "take home messages" will also be provided to the reader particularly focusing on possible clinical implementations and how all this knowledge will very likely bring novelty in the fight against cancer.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19878769     DOI: 10.1016/S0065-230X(09)04001-9

Source DB:  PubMed          Journal:  Adv Cancer Res        ISSN: 0065-230X            Impact factor:   6.242


  5 in total

1.  Time-dependent decrease of clusterin as a potential cerebrospinal fluid biomarker for drug-resistant epilepsy.

Authors:  Weihua Yu; Dan Chen; Zhihua Wang; Chunlei Zhou; Jing Luo; Yali Xu; Lan Shen; Huan Yin; Shuxin Tao; Zheng Xiao; Fei Xiao; Yang Lü; Xuefeng Wang
Journal:  J Mol Neurosci       Date:  2014-02-02       Impact factor: 3.444

2.  Cerebrospinal fluid biomarkers of neuropathologically diagnosed Parkinson's disease subjects.

Authors:  Chera L Maarouf; Thomas G Beach; Charles H Adler; Holly A Shill; Marwan N Sabbagh; Terence Wu; Douglas G Walker; Tyler A Kokjohn; Alex E Roher
Journal:  Neurol Res       Date:  2012-09       Impact factor: 2.448

3.  Effects of female sex hormones on clusterin expression and paclitaxel resistance in endometrial cancer cell lines.

Authors:  Yong Sung Won; Sung Jong Lee; Seung Geun Yeo; Dong Choon Park
Journal:  Int J Med Sci       Date:  2011-12-11       Impact factor: 3.738

4.  Hypoxia inducible factor-1α directly regulates nuclear clusterin transcription by interacting with hypoxia response elements in the clusterin promoter.

Authors:  Jeongsook Park; So Yun Park; Eunkyung Shin; Sun Hee Lee; Yoon Sook Kim; Dong Hoon Lee; Gu Seob Roh; Hyun Joon Kim; Sang Soo Kang; Gyeong Jae Cho; Bo-Young Jeong; Hwajin Kim; Wan Sung Choi
Journal:  Mol Cells       Date:  2014-02-19       Impact factor: 5.034

5.  Assessment of lipocalin 2, clusterin, soluble tumor necrosis factor receptor-1, interleukin-6, homocysteine, and uric acid levels in patients with psoriasis.

Authors:  Arzu Ataseven; Recep Kesli; Gulcan Saylam Kurtipek; Perihan Ozturk
Journal:  Dis Markers       Date:  2014-04-02       Impact factor: 3.434

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.