Hemiprotonic ph-ph + with two targets inhibits metastatic breast cancer and concurrent candidiasis
Concurrent infection in breast cancer patients is the direct cause of the high mortality rate of the disease. However, there is no available method to increase the survival rate until now. To address the problem, we propose one drug with two target strategy to treat the refractory disease. A small c...
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Veröffentlicht in: | Biochemical pharmacology 2024-08, Vol.226, p.116394 |
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creator | Li, Jingli Zhao, Zizhen You, Dongmei Xie, Yafang Feng, Yixiao Li, Xiaorong Cui, Zhihong Fuai, Ling |
description | Concurrent infection in breast cancer patients is the direct cause of the high mortality rate of the disease. However, there is no available method to increase the survival rate until now. To address the problem, we propose one drug with two target strategy to treat the refractory disease. A small chemical, ph-ph
, was attempted to be used in the study to explore the feasibility of the approach in anticancer and antifungus at the same time. The results showed that ph-ph
could prevent the proliferation and metastasis of breast cancer cells, and kill C. albicans simultaneously. The molecular mechanism was associated with the activation of an evolutionarily conserved protease CLpP in the cancer and C. albicans cells. Also, the signaling pathway mediated by PLAGL2 that highly expressed in cancer cells participated in preventing cell metastasis and inducing apoptosis of ph-ph
. The one drug with dual targets inhibited the growth and metastasis of the cancer cells, and meanwhile eliminated C. albicans in tissues in the experimental animals. The results suggested that ph-ph
with dual targets of CLpP and PLAGL2 would be a feasible approach to prolong the survival rate in patients with metastatic breast cancer and pathogenic infection. |
doi_str_mv | 10.1016/j.bcp.2024.116394 |
format | Article |
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, was attempted to be used in the study to explore the feasibility of the approach in anticancer and antifungus at the same time. The results showed that ph-ph
could prevent the proliferation and metastasis of breast cancer cells, and kill C. albicans simultaneously. The molecular mechanism was associated with the activation of an evolutionarily conserved protease CLpP in the cancer and C. albicans cells. Also, the signaling pathway mediated by PLAGL2 that highly expressed in cancer cells participated in preventing cell metastasis and inducing apoptosis of ph-ph
. The one drug with dual targets inhibited the growth and metastasis of the cancer cells, and meanwhile eliminated C. albicans in tissues in the experimental animals. The results suggested that ph-ph
with dual targets of CLpP and PLAGL2 would be a feasible approach to prolong the survival rate in patients with metastatic breast cancer and pathogenic infection.</description><identifier>ISSN: 1873-2968</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/j.bcp.2024.116394</identifier><identifier>PMID: 38942090</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Antifungal Agents - pharmacology ; Antifungal Agents - therapeutic use ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Candida albicans - drug effects ; Candidiasis - drug therapy ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Endopeptidase Clp - antagonists & inhibitors ; Endopeptidase Clp - genetics ; Endopeptidase Clp - metabolism ; Female ; Humans ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Neoplasm Metastasis</subject><ispartof>Biochemical pharmacology, 2024-08, Vol.226, p.116394</ispartof><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38942090$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Jingli</creatorcontrib><creatorcontrib>Zhao, Zizhen</creatorcontrib><creatorcontrib>You, Dongmei</creatorcontrib><creatorcontrib>Xie, Yafang</creatorcontrib><creatorcontrib>Feng, Yixiao</creatorcontrib><creatorcontrib>Li, Xiaorong</creatorcontrib><creatorcontrib>Cui, Zhihong</creatorcontrib><creatorcontrib>Fuai, Ling</creatorcontrib><title>Hemiprotonic ph-ph + with two targets inhibits metastatic breast cancer and concurrent candidiasis</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><description>Concurrent infection in breast cancer patients is the direct cause of the high mortality rate of the disease. However, there is no available method to increase the survival rate until now. To address the problem, we propose one drug with two target strategy to treat the refractory disease. A small chemical, ph-ph
, was attempted to be used in the study to explore the feasibility of the approach in anticancer and antifungus at the same time. The results showed that ph-ph
could prevent the proliferation and metastasis of breast cancer cells, and kill C. albicans simultaneously. The molecular mechanism was associated with the activation of an evolutionarily conserved protease CLpP in the cancer and C. albicans cells. Also, the signaling pathway mediated by PLAGL2 that highly expressed in cancer cells participated in preventing cell metastasis and inducing apoptosis of ph-ph
. The one drug with dual targets inhibited the growth and metastasis of the cancer cells, and meanwhile eliminated C. albicans in tissues in the experimental animals. The results suggested that ph-ph
with dual targets of CLpP and PLAGL2 would be a feasible approach to prolong the survival rate in patients with metastatic breast cancer and pathogenic infection.</description><subject>Animals</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Candida albicans - drug effects</subject><subject>Candidiasis - drug therapy</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Endopeptidase Clp - antagonists & inhibitors</subject><subject>Endopeptidase Clp - genetics</subject><subject>Endopeptidase Clp - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Neoplasm Metastasis</subject><issn>1873-2968</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtLxDAUhYMozjj6A9xIloK03jyaJksZ1BEG3My-pOnVZpg-TFIG_73FB7i6H4ePA-cScs0gZ8DU_T6v3Zhz4DJnTAkjT8iS6VJk3Ch9-o8X5CLGPQAordg5WQhtJAcDS1JvsPNjGNLQe0fHNhtbekePPrU0HQeabHjHFKnvW1_7GTpMNiabZrkOOCN1tncYqO0b6obeTSFg_502vvE2-nhJzt7sIeLV712R3dPjbr3Jtq_PL-uHbTYWCrKiZAqNLCUILoRFcAx5w0EWXGsoHLOyRo2uQSi1YUIw6wo0hZXcgBFWrMjtT-285mPCmKrOR4eHg-1xmGIloBSqEILzWb35Vae6w6Yag-9s-Kz-3iK-AIGVZTc</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Li, Jingli</creator><creator>Zhao, Zizhen</creator><creator>You, Dongmei</creator><creator>Xie, Yafang</creator><creator>Feng, Yixiao</creator><creator>Li, Xiaorong</creator><creator>Cui, Zhihong</creator><creator>Fuai, Ling</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>202408</creationdate><title>Hemiprotonic ph-ph + with two targets inhibits metastatic breast cancer and concurrent candidiasis</title><author>Li, Jingli ; Zhao, Zizhen ; You, Dongmei ; Xie, Yafang ; Feng, Yixiao ; Li, Xiaorong ; Cui, Zhihong ; Fuai, Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p560-5716e947403233ae0c1e2d204528805c1a4be8ecde07891331ac5e95a429093a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antifungal Agents - therapeutic use</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Candida albicans - drug effects</topic><topic>Candidiasis - drug therapy</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Endopeptidase Clp - antagonists & inhibitors</topic><topic>Endopeptidase Clp - genetics</topic><topic>Endopeptidase Clp - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Neoplasm Metastasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Jingli</creatorcontrib><creatorcontrib>Zhao, Zizhen</creatorcontrib><creatorcontrib>You, Dongmei</creatorcontrib><creatorcontrib>Xie, Yafang</creatorcontrib><creatorcontrib>Feng, Yixiao</creatorcontrib><creatorcontrib>Li, Xiaorong</creatorcontrib><creatorcontrib>Cui, Zhihong</creatorcontrib><creatorcontrib>Fuai, Ling</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Jingli</au><au>Zhao, Zizhen</au><au>You, Dongmei</au><au>Xie, Yafang</au><au>Feng, Yixiao</au><au>Li, Xiaorong</au><au>Cui, Zhihong</au><au>Fuai, Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemiprotonic ph-ph + with two targets inhibits metastatic breast cancer and concurrent candidiasis</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>2024-08</date><risdate>2024</risdate><volume>226</volume><spage>116394</spage><pages>116394-</pages><issn>1873-2968</issn><eissn>1873-2968</eissn><abstract>Concurrent infection in breast cancer patients is the direct cause of the high mortality rate of the disease. However, there is no available method to increase the survival rate until now. To address the problem, we propose one drug with two target strategy to treat the refractory disease. A small chemical, ph-ph
, was attempted to be used in the study to explore the feasibility of the approach in anticancer and antifungus at the same time. The results showed that ph-ph
could prevent the proliferation and metastasis of breast cancer cells, and kill C. albicans simultaneously. The molecular mechanism was associated with the activation of an evolutionarily conserved protease CLpP in the cancer and C. albicans cells. Also, the signaling pathway mediated by PLAGL2 that highly expressed in cancer cells participated in preventing cell metastasis and inducing apoptosis of ph-ph
. The one drug with dual targets inhibited the growth and metastasis of the cancer cells, and meanwhile eliminated C. albicans in tissues in the experimental animals. The results suggested that ph-ph
with dual targets of CLpP and PLAGL2 would be a feasible approach to prolong the survival rate in patients with metastatic breast cancer and pathogenic infection.</abstract><cop>England</cop><pmid>38942090</pmid><doi>10.1016/j.bcp.2024.116394</doi></addata></record> |
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subjects | Animals Antifungal Agents - pharmacology Antifungal Agents - therapeutic use Antineoplastic Agents - pharmacology Antineoplastic Agents - therapeutic use Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Breast Neoplasms - pathology Candida albicans - drug effects Candidiasis - drug therapy Cell Line, Tumor Cell Proliferation - drug effects Endopeptidase Clp - antagonists & inhibitors Endopeptidase Clp - genetics Endopeptidase Clp - metabolism Female Humans Mice Mice, Inbred BALB C Mice, Nude Neoplasm Metastasis |
title | Hemiprotonic ph-ph + with two targets inhibits metastatic breast cancer and concurrent candidiasis |
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