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Institution

Nottingham Trent University

EducationNottingham, United Kingdom
About: Nottingham Trent University is a education organization based out in Nottingham, United Kingdom. It is known for research contribution in the topics: Population & Addiction. The organization has 4702 authors who have published 12862 publications receiving 307430 citations. The organization is also known as: NTU & Trent Polytechnic.


Papers
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Journal ArticleDOI
18 Aug 2019-Cells
TL;DR: An overview of cancer stem cells, their role in cancer initiation, progression and chemoresistance, and the progress that has been made in the development of CSC targeted therapies are provided.
Abstract: Chemoresistance is a major problem in cancer therapy as cancer cells develop mechanisms that counteract the effect of chemotherapeutic compounds, leading to relapse and the development of more aggressive cancers that contribute to poor prognosis and survival rates of treated patients. Cancer stem cells (CSCs) play a key role in this event. Apart from their slow proliferative property, CSCs have developed a range of cellular processes that involve drug efflux, drug enzymatic inactivation and other mechanisms. In addition, the microenvironment where CSCs evolve (CSC niche), effectively contributes to their role in cancer initiation, progression and chemoresistance. In the CSC niche, immune cells, mesenchymal stem cells (MSCs), endothelial cells and cancer associated fibroblasts (CAFs) contribute to the maintenance of CSC malignancy via the secretion of factors that promote cancer progression and resistance to chemotherapy. Due to these factors that hinder successful cancer therapies, CSCs are a subject of intense research that aims at better understanding of CSC behaviour and at developing efficient targeting therapies. In this review, we provide an overview of cancer stem cells, their role in cancer initiation, progression and chemoresistance, and discuss the progress that has been made in the development of CSC targeted therapies.

105 citations

Journal ArticleDOI
TL;DR: In this article, a finite element approach to determining the possible shapes of a droplet on a fiber was proposed and numerical results for the clam-shell profile were given for several droplet volumes and equilibrium contact angles and the implications of this for droplet stability.
Abstract: The shape of a small liquid drop on a small diameter fiber may be either an axisymmetric barrel shape or it may be a non-axisymmetric clam-shell shape. Experiments show that when the reduced volume, given by the volume of droplet divided by the fiber radius, is large the barrel shape is the preferred conformation, but that as the volume reduces a transition to a clam-shell (pearl) shape occurs. The volume at which this stability transition occurs depends upon the equilibrium contact angle. In this work we review the known solution to Laplace's equation for the barrel shape and consider the link between the profile, the inflexion in the profile and the stability of the droplet. No known solution of Laplace's equation exists for the clam-shell shape droplet. We therefore consider a finite element approach to determining the possible shapes of a droplet on a fiber and give numerical results for the clam-shell profile. The surface free energies for the two types of droplet conformation on a fiber are computed for several droplet volumes and equilibrium contact angles and the implications of this for droplet stability are discussed.

105 citations

Journal ArticleDOI
TL;DR: Rehydration instructions from the product labels were collated and it was observed that none directed the use of water with a temperature >70°C for formula preparation, as specified by the 2008 revised World Health Organization guidelines.

105 citations

Journal ArticleDOI
TL;DR: It is proposed that the membrane trafficking of TG2, and hence its extracellular activity, is linked to TG2 binding to cell-surface HSPG.

105 citations

Journal ArticleDOI
TL;DR: This study has found no evidence of increased oncologic risk associated with fat grafting in women previously treated for breast cancer.
Abstract: Background Currently, there is no clinical evidence of oncologic risk associated with fat grafting, although its safety has been questioned. The authors investigated the risk of relapse associated with fat grafting in women with a history of breast cancer. Methods Of 328 women with previously treated malignant breast disease who underwent fat grafting at the Nottingham Breast Institute, complete data were available for 211 (invasive carcinoma, n = 184; ductal carcinoma in situ, n = 27). Mean follow-up was 88 months after primary cancer surgery and 32 months after fat grafting. Control subjects were matched 2:1 for date of primary cancer operation (within 2 years), age (within 5 years), type of surgery, tumor histology, estrogen receptor status, and disease-free status by time equivalent to that of fat grafting. Final endpoints were tumor recurrence and death. Outcome results were compared with a systematic review of all patients undergoing fat grafting with adequate follow-up reported in the literature. Results No significant excess oncologic events were observed in patients who had fat grafting compared to controls with regard to local (0.95 percent versus 1.90 percent; p = 0.33), regional (0.95 percent versus 0 percent; p = 0.16), and distant recurrences (3.32 percent versus 2.61 percent; p = 0.65). A systematic review identified case series with a total of 1573 women who had fat grafting after primary oncologic breast surgery. The locoregional relapse rate for these patients was 2.92 percent (0.95 percent per year). Conclusion This study has found no evidence of increased oncologic risk associated with fat grafting in women previously treated for breast cancer. Clinical question/level of evidence Risk, II.

105 citations


Authors

Showing all 4806 results

NameH-indexPapersCitations
David L. Kaplan1771944146082
Paul Mitchell146137895659
Matthew Nguyen131129184346
Ian O. Ellis126105175435
Mark D. Griffiths124123861335
Tao Zhang123277283866
Graham J. Hutchings9799544270
Andrzej Cichocki9795241471
Chris Ryan9597134388
Graham Pawelec8957227373
Christopher D. Buckley8844025664
Ester Cerin7827927086
Michael Hofreiter7827120628
Craig E. Banks7756927520
John R. Griffiths7635623179
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202346
2022144
20211,405
20201,278
2019973
2018825