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Correction: In vitro and in vivo antiproliferative activity of organo-nickel SCS-pincer complexes on estrogen responsive MCF7 and MC4L2 breast cancer cells. Effects of amine fragment substitutions on BSA binding and cytotoxicity
Mahboubeh
Hosseini-Kharat
*ab,
Davit
Zargarian
*a,
Ali Mohammad
Alizadeh
*bc,
Kazem
Karami
d,
Maryam
Saeidifar
e,
Solmaz
Khalighfard
f,
Laurent
Dubrulle
a,
Mostafa
Zakariazadeh
g,
Jean-Philippe
Cloutier
a and
Zahra
Sohrabijam
e
aDépartement de Chimie, Université de Montréal, Montréal, Québec H3C 3J7, Canada. E-mail: m.hosseinikharat@gmail.com; zargarian.davit@umontreal.ca
bCancer Research Center, Tehran University of Medical Sciences, Tehran, Iran. E-mail: aalizadeh@sina.tums.ac.ir
cBreast Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran
dDepartment of Chemistry, Isfahan University of Technology, Isfahan 84156-83111, Iran
eDepartment of Nanotechnology and Advanced Materials, Materials and Energy Research Center, Karaj, Iran
fDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran
gResearch Institute for Fundamental Sciences (RIFS), University of Tabriz, Tabriz, Iran
First published on 13th September 2023
Abstract
Correction for ‘In vitro and in vivo antiproliferative activity of organo-nickel SCS-pincer complexes on estrogen responsive MCF7 and MC4L2 breast cancer cells. Effects of amine fragment substitutions on BSA binding and cytotoxicity’ by Mahboubeh Hosseini-Kharat et al., Dalton Trans., 2018, 47, 16944–16957, https://doi.org/10.1039/c8dt03079k.
In the published version of the above manuscript, the authors noticed that some panels of the images used for Fig. 10 belonged to another published study.1
The authors have now provided a corrected version of Fig. 10, as shown here.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
References
- V. Khori, A. M. Alizadeh, S. Khalighfard, Y. Heidarian and H. Khodayari, Peptides, 2018, 107, 54–60, DOI:10.1016/j.peptides.2018.07.007.
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