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Natural small molecule self-assembled hydrogel inhibited tumor growth and lung metastasis of 4T1 breast cancer by regulating the CXCL1/2-S100A8/9 axis
[Display omitted] •The natural small molecule self-assembled hydrogel of GK-GA was designed in a one-step “green” approach for breast cancer treatments.•The inhibition rate of tumor growth (IRG) of GK-GA was over 90 % at 6.25 mg·kg−1 without any obvious toxicity.•GK-GA hydrogel inhibited breast canc...
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Published in: | Materials & design 2023-01, Vol.225, p.111435, Article 111435 |
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creator | Yang, Yuqin Cai, Desheng Shu, Yisong Yuan, Zhihua Pi, Wenmin Zhang, Yaozhi Lu, Jihui Jiao, Jingyi Cheng, Xuehao Li, Feifei Wang, Penglong Lei, Haimin |
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•The natural small molecule self-assembled hydrogel of GK-GA was designed in a one-step “green” approach for breast cancer treatments.•The inhibition rate of tumor growth (IRG) of GK-GA was over 90 % at 6.25 mg·kg−1 without any obvious toxicity.•GK-GA hydrogel inhibited breast cancer growth and metastasis via dual pathways of BCL2-CASP3 and CXCL1/2-S100A8/9.
It is crucial to inhibit tumor growth and distant metastasis for breast cancer (BC) therapy. However, the treatment primarily dependent on surgery, chemotherapy, and radiotherapy is far from satisfactory. It had been demonstrated that the CXCL1/2-S100A8/9 axis played an essential role in BC therapy. Therefore, we constructed a natural product hydrogel for BC therapy by blocking CXCL1 signaling. The GK-GA (phytochemicals of Genkwa Flos-glycyrrhizic acid) hydrogel was designed in a one-step “green” approach. The pharmacodynamics study showed GK-GA exhibited significant anti-tumor and anti-lung metastasis activities, resulting in the inhibition rate of tumor growth (IRG) over 90 % at 6.25 mg·kg−1, and did not display any obvious toxicity. In addition, the potent antitumor efficiency was also attributed to aggregation/assembly-induced retention (AIR) property. RNA sequencing analysis revealed the gene expression was significantly down-regulated in the GK-GA group, which were BCL2, CASP3, CXCL1, CXCL2, CXCR2, S100A8, S100A9, and confirmed further by western blot (WB). Our findings indicated natural product GK-GA hydrogel inhibited tumor growth and lung metastasis via the BCL2-CASP3 mitochondrial apoptosis pathway as well as the CXCL1/2-S100A8/9 pathway. This study provides inspiration for the fabrication of new excipients-free nano-dispersion in a one-step, no‐carrier‐added, organic solvent-free, “green” approach, particularly for small molecular antitumor agents. |
doi_str_mv | 10.1016/j.matdes.2022.111435 |
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•The natural small molecule self-assembled hydrogel of GK-GA was designed in a one-step “green” approach for breast cancer treatments.•The inhibition rate of tumor growth (IRG) of GK-GA was over 90 % at 6.25 mg·kg−1 without any obvious toxicity.•GK-GA hydrogel inhibited breast cancer growth and metastasis via dual pathways of BCL2-CASP3 and CXCL1/2-S100A8/9.
It is crucial to inhibit tumor growth and distant metastasis for breast cancer (BC) therapy. However, the treatment primarily dependent on surgery, chemotherapy, and radiotherapy is far from satisfactory. It had been demonstrated that the CXCL1/2-S100A8/9 axis played an essential role in BC therapy. Therefore, we constructed a natural product hydrogel for BC therapy by blocking CXCL1 signaling. The GK-GA (phytochemicals of Genkwa Flos-glycyrrhizic acid) hydrogel was designed in a one-step “green” approach. The pharmacodynamics study showed GK-GA exhibited significant anti-tumor and anti-lung metastasis activities, resulting in the inhibition rate of tumor growth (IRG) over 90 % at 6.25 mg·kg−1, and did not display any obvious toxicity. In addition, the potent antitumor efficiency was also attributed to aggregation/assembly-induced retention (AIR) property. RNA sequencing analysis revealed the gene expression was significantly down-regulated in the GK-GA group, which were BCL2, CASP3, CXCL1, CXCL2, CXCR2, S100A8, S100A9, and confirmed further by western blot (WB). Our findings indicated natural product GK-GA hydrogel inhibited tumor growth and lung metastasis via the BCL2-CASP3 mitochondrial apoptosis pathway as well as the CXCL1/2-S100A8/9 pathway. This study provides inspiration for the fabrication of new excipients-free nano-dispersion in a one-step, no‐carrier‐added, organic solvent-free, “green” approach, particularly for small molecular antitumor agents.</description><identifier>ISSN: 0264-1275</identifier><identifier>EISSN: 1873-4197</identifier><identifier>DOI: 10.1016/j.matdes.2022.111435</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>4T1 breast cancer ; Anti-lung metastasis ; CXCL1/2-S100A8/9 axis ; Inhibit tumor growth ; Natural small molecule self-assembled hydrogel</subject><ispartof>Materials & design, 2023-01, Vol.225, p.111435, Article 111435</ispartof><rights>2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-735fae943703b950bd6542de4b5b637a042377614e917523b3a3e987224d02b83</citedby><cites>FETCH-LOGICAL-c418t-735fae943703b950bd6542de4b5b637a042377614e917523b3a3e987224d02b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Yang, Yuqin</creatorcontrib><creatorcontrib>Cai, Desheng</creatorcontrib><creatorcontrib>Shu, Yisong</creatorcontrib><creatorcontrib>Yuan, Zhihua</creatorcontrib><creatorcontrib>Pi, Wenmin</creatorcontrib><creatorcontrib>Zhang, Yaozhi</creatorcontrib><creatorcontrib>Lu, Jihui</creatorcontrib><creatorcontrib>Jiao, Jingyi</creatorcontrib><creatorcontrib>Cheng, Xuehao</creatorcontrib><creatorcontrib>Li, Feifei</creatorcontrib><creatorcontrib>Wang, Penglong</creatorcontrib><creatorcontrib>Lei, Haimin</creatorcontrib><title>Natural small molecule self-assembled hydrogel inhibited tumor growth and lung metastasis of 4T1 breast cancer by regulating the CXCL1/2-S100A8/9 axis</title><title>Materials & design</title><description>[Display omitted]
•The natural small molecule self-assembled hydrogel of GK-GA was designed in a one-step “green” approach for breast cancer treatments.•The inhibition rate of tumor growth (IRG) of GK-GA was over 90 % at 6.25 mg·kg−1 without any obvious toxicity.•GK-GA hydrogel inhibited breast cancer growth and metastasis via dual pathways of BCL2-CASP3 and CXCL1/2-S100A8/9.
It is crucial to inhibit tumor growth and distant metastasis for breast cancer (BC) therapy. However, the treatment primarily dependent on surgery, chemotherapy, and radiotherapy is far from satisfactory. It had been demonstrated that the CXCL1/2-S100A8/9 axis played an essential role in BC therapy. Therefore, we constructed a natural product hydrogel for BC therapy by blocking CXCL1 signaling. The GK-GA (phytochemicals of Genkwa Flos-glycyrrhizic acid) hydrogel was designed in a one-step “green” approach. The pharmacodynamics study showed GK-GA exhibited significant anti-tumor and anti-lung metastasis activities, resulting in the inhibition rate of tumor growth (IRG) over 90 % at 6.25 mg·kg−1, and did not display any obvious toxicity. In addition, the potent antitumor efficiency was also attributed to aggregation/assembly-induced retention (AIR) property. RNA sequencing analysis revealed the gene expression was significantly down-regulated in the GK-GA group, which were BCL2, CASP3, CXCL1, CXCL2, CXCR2, S100A8, S100A9, and confirmed further by western blot (WB). Our findings indicated natural product GK-GA hydrogel inhibited tumor growth and lung metastasis via the BCL2-CASP3 mitochondrial apoptosis pathway as well as the CXCL1/2-S100A8/9 pathway. This study provides inspiration for the fabrication of new excipients-free nano-dispersion in a one-step, no‐carrier‐added, organic solvent-free, “green” approach, particularly for small molecular antitumor agents.</description><subject>4T1 breast cancer</subject><subject>Anti-lung metastasis</subject><subject>CXCL1/2-S100A8/9 axis</subject><subject>Inhibit tumor growth</subject><subject>Natural small molecule self-assembled hydrogel</subject><issn>0264-1275</issn><issn>1873-4197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kdtq3DAQhk1poNskb5ALvYB3dbJl3xTC0kNgSS6aQu_EyBp5tcjrIslt90X6vFXq0svCwMDPzDeHv6ruGN0yytrdaTtBtpi2nHK-ZYxJ0byqNqxTopasV6-rDeWtrBlXzZvqbUonWgqVkJvq1yPkJUIgaYIQyDQHHJaAJGFwNaSEkwloyfFi4zxiIP589MbnIuVlmiMZ4_wjHwmcLQnLeSQTZkglfCKzI_KZEROxKGSA84CRmAuJOC4Bsi_V-Yhk_3V_YDtef2aU3ne7nsBPn26qKwch4e3ffF19-fD-ef-pPjx9fNjfH-pBsi7XSjQOsJdCUWH6hhrbNpJblKYxrVBAJRdKtUxiz1TDhREgsO8U59JSbjpxXT2sXDvDSX-LfoJ40TN4_UeY46ghZj8E1E4w2VguuXNlIGDnOmWFlJb33AnRFpZcWUOcU4ro_vEY1S8-6ZNefdIvPunVp9L2bm3Dcud3j1GnwWN5lvURh1wW8f8H_AbpXZxi</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Yang, Yuqin</creator><creator>Cai, Desheng</creator><creator>Shu, Yisong</creator><creator>Yuan, Zhihua</creator><creator>Pi, Wenmin</creator><creator>Zhang, Yaozhi</creator><creator>Lu, Jihui</creator><creator>Jiao, Jingyi</creator><creator>Cheng, Xuehao</creator><creator>Li, Feifei</creator><creator>Wang, Penglong</creator><creator>Lei, Haimin</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>202301</creationdate><title>Natural small molecule self-assembled hydrogel inhibited tumor growth and lung metastasis of 4T1 breast cancer by regulating the CXCL1/2-S100A8/9 axis</title><author>Yang, Yuqin ; Cai, Desheng ; Shu, Yisong ; Yuan, Zhihua ; Pi, Wenmin ; Zhang, Yaozhi ; Lu, Jihui ; Jiao, Jingyi ; Cheng, Xuehao ; Li, Feifei ; Wang, Penglong ; Lei, Haimin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-735fae943703b950bd6542de4b5b637a042377614e917523b3a3e987224d02b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>4T1 breast cancer</topic><topic>Anti-lung metastasis</topic><topic>CXCL1/2-S100A8/9 axis</topic><topic>Inhibit tumor growth</topic><topic>Natural small molecule self-assembled hydrogel</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Yuqin</creatorcontrib><creatorcontrib>Cai, Desheng</creatorcontrib><creatorcontrib>Shu, Yisong</creatorcontrib><creatorcontrib>Yuan, Zhihua</creatorcontrib><creatorcontrib>Pi, Wenmin</creatorcontrib><creatorcontrib>Zhang, Yaozhi</creatorcontrib><creatorcontrib>Lu, Jihui</creatorcontrib><creatorcontrib>Jiao, Jingyi</creatorcontrib><creatorcontrib>Cheng, Xuehao</creatorcontrib><creatorcontrib>Li, Feifei</creatorcontrib><creatorcontrib>Wang, Penglong</creatorcontrib><creatorcontrib>Lei, Haimin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>Directory of Open Access Journals</collection><jtitle>Materials & design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Yuqin</au><au>Cai, Desheng</au><au>Shu, Yisong</au><au>Yuan, Zhihua</au><au>Pi, Wenmin</au><au>Zhang, Yaozhi</au><au>Lu, Jihui</au><au>Jiao, Jingyi</au><au>Cheng, Xuehao</au><au>Li, Feifei</au><au>Wang, Penglong</au><au>Lei, Haimin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural small molecule self-assembled hydrogel inhibited tumor growth and lung metastasis of 4T1 breast cancer by regulating the CXCL1/2-S100A8/9 axis</atitle><jtitle>Materials & design</jtitle><date>2023-01</date><risdate>2023</risdate><volume>225</volume><spage>111435</spage><pages>111435-</pages><artnum>111435</artnum><issn>0264-1275</issn><eissn>1873-4197</eissn><abstract>[Display omitted]
•The natural small molecule self-assembled hydrogel of GK-GA was designed in a one-step “green” approach for breast cancer treatments.•The inhibition rate of tumor growth (IRG) of GK-GA was over 90 % at 6.25 mg·kg−1 without any obvious toxicity.•GK-GA hydrogel inhibited breast cancer growth and metastasis via dual pathways of BCL2-CASP3 and CXCL1/2-S100A8/9.
It is crucial to inhibit tumor growth and distant metastasis for breast cancer (BC) therapy. However, the treatment primarily dependent on surgery, chemotherapy, and radiotherapy is far from satisfactory. It had been demonstrated that the CXCL1/2-S100A8/9 axis played an essential role in BC therapy. Therefore, we constructed a natural product hydrogel for BC therapy by blocking CXCL1 signaling. The GK-GA (phytochemicals of Genkwa Flos-glycyrrhizic acid) hydrogel was designed in a one-step “green” approach. The pharmacodynamics study showed GK-GA exhibited significant anti-tumor and anti-lung metastasis activities, resulting in the inhibition rate of tumor growth (IRG) over 90 % at 6.25 mg·kg−1, and did not display any obvious toxicity. In addition, the potent antitumor efficiency was also attributed to aggregation/assembly-induced retention (AIR) property. RNA sequencing analysis revealed the gene expression was significantly down-regulated in the GK-GA group, which were BCL2, CASP3, CXCL1, CXCL2, CXCR2, S100A8, S100A9, and confirmed further by western blot (WB). Our findings indicated natural product GK-GA hydrogel inhibited tumor growth and lung metastasis via the BCL2-CASP3 mitochondrial apoptosis pathway as well as the CXCL1/2-S100A8/9 pathway. This study provides inspiration for the fabrication of new excipients-free nano-dispersion in a one-step, no‐carrier‐added, organic solvent-free, “green” approach, particularly for small molecular antitumor agents.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.matdes.2022.111435</doi><oa>free_for_read</oa></addata></record> |
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subjects | 4T1 breast cancer Anti-lung metastasis CXCL1/2-S100A8/9 axis Inhibit tumor growth Natural small molecule self-assembled hydrogel |
title | Natural small molecule self-assembled hydrogel inhibited tumor growth and lung metastasis of 4T1 breast cancer by regulating the CXCL1/2-S100A8/9 axis |
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