Theranostic Lysosomal Targeting Anticancer and Antimetastatic Agents: Half-Sandwich Iridium(III) Rhodamine Complexes
Identifieur interne : 000A51 ( Ncbi/Checkpoint ); précédent : 000A50; suivant : 000A52Theranostic Lysosomal Targeting Anticancer and Antimetastatic Agents: Half-Sandwich Iridium(III) Rhodamine Complexes
Auteurs : Wenli Ma [République populaire de Chine] ; Xingxing Ge [République populaire de Chine] ; Zhishan Xu [République populaire de Chine] ; Shumiao Zhang [République populaire de Chine] ; Xiangdong He [République populaire de Chine] ; Juanjuan Li [République populaire de Chine] ; Xiaorong Xia [République populaire de Chine] ; Xiaobing Chen [République populaire de Chine] ; Zhe Liu [République populaire de Chine]Source :
- ACS Omega [ 2470-1343 ] ; 2019.
Abstract
Two rhodamine-modified half-sandwich
Ir(III) complexes with the
general formula [(Cpx)Ir(ĈN) Cl] were synthesized
and characterized, where Cpx is 1-biphenyl-2,3,4,5-tetramethylcyclopentadienyl
(Cpxbiph). Both complexes showed potent anticancer activity
against A549, HeLa, and HepG2 cancer cells and normal cells, and altered
ligands had an effect on proliferation resistance. The complex enters
cells through energy dependence, and because of the different ligands,
not only could it affect the anticancer ability of the complex but
also could affect the degree of complex lysosome targeting, lysosomal
damage, and further prove the antiproliferative mechanism of the complex.
Excitingly, antimetastatic experiments demonstrated that complex
Url:
DOI: 10.1021/acsomega.9b01863
PubMed: 31552370
PubMed Central: 6751730
Affiliations:
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<author><name sortKey="Ge, Xingxing" sort="Ge, Xingxing" uniqKey="Ge X" first="Xingxing" last="Ge">Xingxing Ge</name>
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, Qufu 273165,<country>China</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Zhang, Shumiao" sort="Zhang, Shumiao" uniqKey="Zhang S" first="Shumiao" last="Zhang">Shumiao Zhang</name>
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<author><name sortKey="Li, Juanjuan" sort="Li, Juanjuan" uniqKey="Li J" first="Juanjuan" last="Li">Juanjuan Li</name>
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, Qufu 273165,<country>China</country>
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<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<author><name sortKey="Xia, Xiaorong" sort="Xia, Xiaorong" uniqKey="Xia X" first="Xiaorong" last="Xia">Xiaorong Xia</name>
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<author><name sortKey="Chen, Xiaobing" sort="Chen, Xiaobing" uniqKey="Chen X" first="Xiaobing" last="Chen">Xiaobing Chen</name>
<affiliation wicri:level="1"><nlm:aff id="aff1">Institute of Anticancer Agents Development and Theranostic Application, The Key Laboratory of Life-Organic Analysis and Key Laboratory of Pharmaceutical Intermediates and Analysis of Natural Medicine, Department of Chemistry and Chemical Engineering,<institution>Qufu Normal University</institution>
, Qufu 273165,<country>China</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Liu, Zhe" sort="Liu, Zhe" uniqKey="Liu Z" first="Zhe" last="Liu">Zhe Liu</name>
<affiliation wicri:level="1"><nlm:aff id="aff1">Institute of Anticancer Agents Development and Theranostic Application, The Key Laboratory of Life-Organic Analysis and Key Laboratory of Pharmaceutical Intermediates and Analysis of Natural Medicine, Department of Chemistry and Chemical Engineering,<institution>Qufu Normal University</institution>
, Qufu 273165,<country>China</country>
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<series><title level="j">ACS Omega</title>
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<front><div type="abstract" xml:lang="en"><p content-type="toc-graphic"><graphic xlink:href="ao9b01863_0013" id="ab-tgr1"></graphic>
</p>
<p>Two rhodamine-modified half-sandwich
Ir(III) complexes with the
general formula [(Cp<sup>x</sup>
)Ir(ĈN) Cl] were synthesized
and characterized, where Cp<sup>x</sup>
is 1-biphenyl-2,3,4,5-tetramethylcyclopentadienyl
(Cp<sup>xbiph</sup>
). Both complexes showed potent anticancer activity
against A549, HeLa, and HepG2 cancer cells and normal cells, and altered
ligands had an effect on proliferation resistance. The complex enters
cells through energy dependence, and because of the different ligands,
not only could it affect the anticancer ability of the complex but
also could affect the degree of complex lysosome targeting, lysosomal
damage, and further prove the antiproliferative mechanism of the complex.
Excitingly, antimetastatic experiments demonstrated that complex <bold>1</bold>
has the ability to block the migration of cancer cells.
Furthermore, although the complex did not show a stronger ability
to interfere with the coenzyme NAD<sup>+</sup>
/NADH pair by transfer
hydrogenation, the intracellular reactive oxygen species (ROS) content
has shown a marked increase. NF-κB activity is increased by
ROS regulation, and the role of ROS-NF-κB signaling pathway
further induces apoptosis. Moreover, cell flow experiments also demonstrated
that complex <bold>1</bold>
blocked the cell cycle in S phase, but
the complex did not cause significant changes in the mitochondrial
membrane potential.</p>
</div>
</front>
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<name sortKey="Xia, Xiaorong" sort="Xia, Xiaorong" uniqKey="Xia X" first="Xiaorong" last="Xia">Xiaorong Xia</name>
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</record>
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