{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T15:52:18Z","timestamp":1753890738956,"version":"3.41.2"},"reference-count":44,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2022,7,13]],"date-time":"2022-07-13T00:00:00Z","timestamp":1657670400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Chem."],"abstract":"<jats:p>In the continuous effort to find new metal-based compounds as alternatives to platinum-related anticancer drugs, 11<jats:sup>th<\/jats:sup> group metal phosphane compounds have been thoroughly taken into consideration. Tris-arylphosphane metal derivatives have been extensively considered as heteroleptic metal compounds exhibiting remarkable cytotoxic activities. Functional groups in the aryl moieties modulate the activity reinforcing or eliminating it. Previous works have highlighted that the presence of hydrophilic groups in the phosphane ligands, such as COOH or OH, hampers the anticancer activity of gold azolate\/PPh<jats:sub>3<\/jats:sub> compounds. To increase the polarity of the triarylphosphane ligand without affecting the activity, we considered the preparation of esters starting from the 4-diphenylphosphane-benzoic acid. The resulting phosphanes are poorer donators than the PPh<jats:sub>3<\/jats:sub>, leading to poly-phosphane M(I) compounds, and they exhibit intense emissive properties. A homologous series of L<jats:sub>3<\/jats:sub>MX-type compounds (where M = Au and X = Cl, M = Cu and X = BF<jats:sub>4<\/jats:sub>, and M = Ag and X = PF<jats:sub>6<\/jats:sub>) were obtained with the 4-methoxy-diphenylphosphane benzoate. The homologous metal compounds have been characterized by analytical and spectroscopic methods and, remarkably, their formation was associated with high frequencies of <jats:sup>31<\/jats:sup>P NMR chemical shift variations (5\u201335\u00a0ppm in CDCl<jats:sub>3<\/jats:sub>). The new complexes and the ligand were evaluated on sensitive and cisplatin-resistant human tumor cell lines. The ligand is ineffective on cells while the complexes exert a notable antiproliferative effect. The homologous series of the L<jats:sub>3<\/jats:sub>MX complexes were able to significantly reduce the cell viability of human triple-negative breast cancer cells (MDA-MB-231), representing the most aggressive subtype of breast cancer, and of ovarian carcinoma (A2780). Among these coinage metal compounds, L<jats:sub>3<\/jats:sub>AgPF<jats:sub>6<\/jats:sub> results the most interesting, showing the lowest GI<jats:sub>50<\/jats:sub> values in all cell lines. Interestingly, this silver complex is more cytotoxic than cisplatin, taken as reference drug. The investigation of the mechanism of action of L<jats:sub>3<\/jats:sub>AgPF<jats:sub>6<\/jats:sub> in A2780 cells highlighted the induction of the apoptotic pathway, the depolarization of the mitochondrial inner membrane, and a significant accumulation in cells.<\/jats:p>","DOI":"10.3389\/fchem.2022.924584","type":"journal-article","created":{"date-parts":[[2022,7,13]],"date-time":"2022-07-13T04:40:56Z","timestamp":1657687256000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":2,"title":["Coinage Metal Compounds With 4-Methoxy-Diphenylphosphane Benzoate Ligand Inhibit Female Cancer Cell Growth"],"prefix":"10.3389","volume":"10","author":[{"given":"Lorenzo","family":"Luciani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rossana","family":"Galassi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Junbiao","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cristina","family":"Marchini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alessia","family":"Cogo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria Luisa","family":"Di Paolo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lisa","family":"Dalla Via","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2022,7,13]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"12888","DOI":"10.1039\/D0SC04082G","article-title":"Metallodrugs are Unique: Opportunities and Challenges of Discovery and Development","volume":"11","author":"Anthony","year":"2020","journal-title":"Chem. 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