Efficient Delivery of GSDMD‐N mRNA by Engineered Extracellular Vesicles Induces Pyroptosis for Enhanced Immunotherapy
Open accessAbstract
Pyroptosis is a newly discovered inflammatory form of programmed cell death, which promotes systemic immune response in cancer immunotherapy. GSDMD is one of the key molecules executing pyroptosis, while therapeutical delivery of GSDMD to tumor cells is of great challenge. In this study, an extracellular vesicles‐based GSDMD‐N mRNA delivery system (namely EV Tx ) is developed for enhanced cancer immunotherapy, with GSDMD‐N mRNA encapsulated inside, Ce6 (Chlorin e6 (Ce6), a hydrophilic sensitizer) incorporated into extracellular vesicular membrane, and HER2 antibody displayed onto the surface. Briefly, GSDMD‐N mRNA is translationally repressed in donor cells by optimized puromycin, ensuring the cell viability and facilitating the mRNA encapsulation into extracellular vesicles. When targeted and delivered into HER2 + breast cancer cells by the engineered extracellular vesicles, the translational repression is unleashed in the recipient cells as the puromycin is diluted and additionally inactivated by sonodynamic treatment as the extracellular vesicles are armed with Ce6, allowing GSDMD‐N translation and pyroptosis induction. In addition, sonodynamic treatment also induces cell death in the recipient cells. In the SKBR3‐ and HER2 transfected 4T1‐ inoculated breast tumor mouse models, the engineered EV Tx efficiently induces a powerful tumor immune response and suppressed tumor growth, providing a nanoplatform for cancer immunotherapy.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
EVTx system transporting GSDMD-N mRNA successfully reversed translational repression upon delivery to HER2-positive breast tumor cells.
“Upon delivery to HER2-positive breast tumor cells, this engineered system successfully reversed translational repression.”
From Exosome for mRNA delivery: Strategies and therapeutic applications (2024) · cites this paper as [127]
EVTx exerted additional therapeutic mechanism by triggering apoptosis in cancer cells through sonodynamic therapy.
“Furthermore, it exerted an additional therapeutic mechanism by triggering apoptosis in cancer cells through the application of sonodynamic therapy [127].”
From Exosome for mRNA delivery: Strategies and therapeutic applications (2024) · cites this paper as [127]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The blockade of immune checkpoints in cancer immunotherapy
Pardoll, D. M. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3239 · Cited by 13,838 · see citing works
The biology <b>,</b> function <b>,</b> and biomedical applications of exosomes
Kalluri, R., & LeBleu, V. S. (2020) · Science · doi:10.1126/science.aau6977 · Cited by 10,770 · see citing works
Oncology meets immunology: the cancer-immunity cycle.
Chen, D. S., & Mellman, I. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.012 · Cited by 6,929 · see citing works
Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death
Shi, J., Zhao, Y., Wang, K., Shi, X., Wang, Y., Huang, H., Zhuang, Y., Cai, T., Wang, F., & Shao, F. (2015) · Nature · doi:10.1038/nature15514 · Cited by 6,659 · see citing works
Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
Kayagaki, N., Stowe, I. B., Lee, B. L., O’Rourke, K., Anderson, K., Warming, S., Cuellar, T., Haley, B., Roose-Girma, M., Phung, Q. T., et al. (2015) · Nature · doi:10.1038/nature15541 · Cited by 3,686 · see citing works
Chemotherapy drugs induce pyroptosis through caspase-3 cleavage of a gasdermin
Wang, Y., Gao, W., Shi, X., Ding, J., Liu, W., He, H., Wang, K., & Shao, F. (2017) · Nature · doi:10.1038/nature22393 · Cited by 3,199 · see citing works
Pyroptosis: Gasdermin-Mediated Programmed Necrotic Cell Death
Shi, J., Gao, W., & Shao, F. (2017) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.10.004 · Cited by 3,088 · see citing works
Pore-forming activity and structural autoinhibition of the gasdermin family
Ding, J., Wang, K., Liu, W., She, Y., Sun, Q., Shi, J., Sun, H., Wang, D.-C., & Shao, F. (2016) · Nature · doi:10.1038/nature18590 · Cited by 2,771 · see citing works
Tian, Y., Li, S., Song, J., Ji, T., Zhu, M., Anderson, G. J., Wei, J., & Nie, G. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.11.083 · Cited by 1,809 · see citing works
Gasdermin E suppresses tumour growth by activating anti-tumour immunity
Zhang, Z., Zhang, Y., Xia, S., Kong, Q., Li, S., Liu, X., Junqueira, C., Meza‐Sosa, K. F., Mok, T. M. Y., Ansara, J., et al. (2020) · Nature · doi:10.1038/s41586-020-2071-9 · Cited by 1,703 · see citing works
Exosomes: composition, biogenesis, and mechanisms in cancer metastasis and drug resistance
Mashouri, L., Yousefi, H., Aref, A., Ahadi, A., Molaei, F., & Alahari, S. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0991-5 · Cited by 1,345 · see citing works
Exosome Secretion: Molecular Mechanisms and Roles in Immune Responses
Bobrie, A., Colombo, M., Raposo, G., & Théry, C. (2011) · Traffic · doi:10.1111/j.1600-0854.2011.01225.x · Cited by 1,102 · see citing works
A bioorthogonal system reveals antitumour immune function of pyroptosis
Wang, Q., Wang, Y., Ding, J., Wang, C., Zhou, X., Gao, W., Huang, H., Shao, F., & Liu, Z. (2020) · Nature · doi:10.1038/s41586-020-2079-1 · Cited by 1,086 · see citing works
Hou, J., Zhao, R., Xia, W., Chang, C.-W. M., You, Y., Hsu, J.-M., Nie, L., Chen, Y., Wang, Y.-C., Liu, C., et al. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0575-z · Cited by 966 · see citing works
Chen, X., He, W.-T., Hu, L., Li, J., Fang, Y., Wang, X., Xu, X., Wang, Z., Huang, K., & Han, J. (2016) · Cell Research · doi:10.1038/cr.2016.100 · Cited by 831 · see citing works
Nam, J., Son, S., Ochyl, L. J., Kuai, R., Schwendeman, A., & Moon, J. J. (2018) · Nature Communications · doi:10.1038/s41467-018-03473-9 · Cited by 808 · see citing works
Kojima, R., Bojar, D., Rizzi, G., Hamri, G. C.-E., El-Baba, M. D., Saxena, P., Ausländer, S., Tan, K. R., & Fussenegger, M. (2018) · Nature Communications · doi:10.1038/s41467-018-03733-8 · Cited by 748 · see citing works
Succination inactivates gasdermin D and blocks pyroptosis
Humphries, F., Shmuel-Galia, L., Ketelut-Carneiro, N., Li, S., Wang, B.-W., Nemmara, V. V., Wilson, R., Jiang, Z., Khalighinejad, F., Muneeruddin, K., et al. (2020) · Science · doi:10.1126/science.abb9818 · Cited by 627 · see citing works
Deciphering and Reversing Tumor Immune Suppression
Motz, G. T., & Coukos, G. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.005 · Cited by 600 · see citing works
Lai, C. P., Kim, E. Y., Badr, C. E., Weissleder, R., Mempel, T. R., Tannous, B. A., & Breakefield, X. O. (2015) · Nature Communications · doi:10.1038/ncomms8029 · Cited by 574 · see citing works
Self-assembled single-atom nanozyme for enhanced photodynamic therapy treatment of tumor
Wang, D., Wu, H., Phua, S. Z. F., Yang, G., Lim, W. Q., Gu, L., Qian, C., Wang, H., Guo, Z. G., Chen, H., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14199-7 · Cited by 545 · see citing works
Self-citationMechanisms of inflammasome activation: recent advances and novel insights
Vanaja, S. K., Rathinam, V. A. K., & Fitzgerald, K. A. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.12.009 · Cited by 499 · see citing works
Engineered exosomes as an in situ DC-primed vaccine to boost antitumor immunity in breast cancer
Huang, L., Rong, Y., Tang, X., Yi, K., Qi, P., Hou, J., Liu, W., He, Y. Z., Gao, X., Yuan, C., et al. (2022) · Molecular Cancer · doi:10.1186/s12943-022-01515-x · Cited by 413 · see citing works
Weiss, E. S., Girard-Guyonvarc’h, C., Holzinger, D., de Jesus, A. A., Tariq, Z., Picarsic, J. L., Schiffrin, E. J., Foell, D., Grom, A. A., Ammann, S., et al. (2018) · Blood · doi:10.1182/blood-2017-12-820852 · Cited by 396 · see citing works
The metabolite α-KG induces GSDMC-dependent pyroptosis through death receptor 6-activated caspase-8
Zhang, J.-Y., Zhou, B., Sun, R.-Y., Ai, Y.-L., Cheng, K., Li, F.-N., Wang, B.-R., Liu, F.-J., Jiang, Z., Wang, W., et al. (2021) · Cell Research · doi:10.1038/s41422-021-00506-9 · Cited by 392 · see citing works
Cryo-EM structure of the gasdermin A3 membrane pore
Ruan, J., Xia, S., Liu, X., Lieberman, J., & Wu, H. (2018) · Nature · doi:10.1038/s41586-018-0058-6 · Cited by 369 · see citing works
Single-Molecule Imaging Reveals Translation of mRNAs Localized to Stress Granules
Matějů, D., Eichenberger, B., Voigt, F., Eglinger, J., Roth, G., & Chao, J. A. (2020) · Cell · doi:10.1016/j.cell.2020.11.010 · Cited by 341 · see citing works
Genetically Engineered Microvesicles Carrying Suicide mRNA/Protein Inhibit Schwannoma Tumor Growth
Mizrak, A., Bolukbasi, M. F., Ozdener, G. B., Brenner, G. J., Madlener, S., Erkan, E. P., Ströbel, T., Breakefield, X. O., & Saydam, O. (2013) · Molecular Therapy · doi:10.1038/mt.2012.161 · Cited by 337 · see citing works
Pyroptosis at the forefront of anticancer immunity
Loveless, R., Bloomquist, R. F., & Teng, Y. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02065-8 · Cited by 321 · see citing works
Programming cell pyroptosis with biomimetic nanoparticles for solid tumor immunotherapy
Zhao, P., Wang, M., Chen, M., Chen, Z., Peng, X., Zhou, F., Song, J., & Qu, J. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120142 · Cited by 263 · see citing works
mRNA display: from basic principles to macrocycle drug discovery
Josephson, K., Ricardo, A., & Szostak, J. W. (2013) · Drug Discovery Today · doi:10.1016/j.drudis.2013.10.011 · Cited by 209 · see citing works
Heterogeneity of response to immune checkpoint blockade in hypermutated experimental gliomas
Aslan, K., Turco, V., Blobner, J., Sonner, J. K., Liuzzi, A. R., Núñez, N. G., Feo, D. D., Kickingereder, P., Fischer, M. D., Green, E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14642-0 · Cited by 158 · see citing works
Synergistic immunotherapy of glioblastoma by dual targeting of IL-6 and CD40
Yang, F., He, Z., Duan, H., Zhang, D., Li, J., Yang, H., Dorsey, J. F., Zou, W., Nabavizadeh, S. A., Bagley, S. J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23832-3 · Cited by 157 · see citing works
Yang, Z., Zhu, Y., Dong, Z., Li, W., Yang, N., Wang, X., Feng, L., & Liu, Z. (2021) · Nature Communications · doi:10.1038/s41467-021-24604-9 · Cited by 153 · see citing works
Patten, D. K., Corleone, G., Győrffy, B., Perone, Y., Slaven, N., Barozzi, I., Erdős, E., Saiakhova, A., Goddard, K. S., Vingiani, A., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0091-x · Cited by 129 · see citing works
In vivo self-assembled small RNAs as a new generation of RNAi therapeutics
Fu, Z., Zhang, X., Zhou, X., Ur-Rehman, U., Yu, M., Liang, H., Guo, H., Guo, X., Kong, Y., Su, Y., et al. (2021) · Cell Research · doi:10.1038/s41422-021-00491-z · Cited by 128 · see citing works
Kim, G., Lee, Y., Ha, J., Han, S., & Lee, M. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.12.053 · Cited by 120 · see citing works
ZBP1 promotes LPS-induced cell death and IL-1β release via RHIM-mediated interactions with RIPK1
Muendlein, H. I., Connolly, W. M., Magri, Z., Smirnova, I., Ilyukha, V., Gautam, A., Degterev, A., & Poltorak, A. N. (2021) · Nature Communications · doi:10.1038/s41467-020-20357-z · Cited by 108 · see citing works
Qin, Y., Hou, Y., Liu, S., Zhu, P., Wan, X., Zhao, M., Peng, M., Zeng, H., Li, Q., Jin, T., et al. (2020) · Advanced Science · doi:10.1002/advs.202002232 · Cited by 106 · see citing works
Wang, T., Cai, S., Wang, M., Zhang, W., Zhang, K., Chen, D., Li, Z., & Jiang, S. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00010 · Cited by 105 · see citing works
A p53/miR-30a/ZEB2 axis controls triple negative breast cancer aggressiveness
di Gennaro, A., Damiano, V., Brisotto, G., Armellin, M., Perin, T., Zucchetto, A., Guardascione, M., Spaink, H. P., Doglioni, C., Snaar-Jagalska, E. B., et al. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0103-x · Cited by 101 · see citing works
Kim, H. J., Ogura, S., Otabe, T., Kamegawa, R., Sato, M., Kataoka, K., & Miyata, K. (2019) · ACS Central Science · doi:10.1021/acscentsci.9b00843 · Cited by 91 · see citing works
An amphiphilic dendrimer as a light-activable immunological adjuvant for in situ cancer vaccination
Wang, Y., Gong, N., Ma, C., Zhang, Y., Tan, H., Qing, G., Zhang, J., Wang, Y., Wang, J., Chen, S., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25197-z · Cited by 89 · see citing works
Inferring protein expression changes from mRNA in Alzheimer’s dementia using deep neural networks
Tasaki, S., Xu, J., Avey, D. R., Johnson, L., Petyuk, V., Dawe, R. J., Bennett, D. A., Wang, Y., & Gaiteri, C. (2022) · Nature Communications · doi:10.1038/s41467-022-28280-1 · Cited by 84 · see citing works
Li, Z., Zhou, X., Gao, X., Bai, D., Dong, Y., Sun, W., Zhao, L., Wei, M., Yang, X., Yang, G., et al. (2020) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2020.1816710 · Cited by 81 · see citing works
Self-citationZhang, L., Qiang, J., Yang, X., Wang, D., Rehman, A. U., He, X., Chen, W., Sheng, D., Zhou, L., Jiang, Y., et al. (2019) · Advanced Science · doi:10.1002/advs.201901728 · Cited by 66 · see citing works
Yin, Q., Pan, A., Chen, B., Wang, Z., Tang, M., Yan, Y., Wang, Y., Xia, H., Chen, W., Du, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22678-z · Cited by 52 · see citing works
Cyclophilin A promotes cell migration via the Abl-Crk signaling pathway
Saleh, T., Jankowski, W., Sriram, G., Rossi, P., Shah, S., Lee, K., Cruz, L. A., Rodriguez, A. J., Birge, R. B., & Kalodimos, C. G. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1981 · Cited by 42 · see citing works
Ouyang, Q., Yan, B., Li, A., Hu, Z.-S., Feng, J., Lun, X.-X., Zhang, M., Zhang, M., Wu, K., Xue, F., et al. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.06.016 · Cited by 13 · see citing works
Self-citation
Flagged first, then by citations
3 of the 52 references couldn’t be matched to a known paper.
Research works printed but not linked: 49
- A. di Gennaro, V. Damiano, G. Brisotto, M. Armellin, T. Perin, A. Zucchetto, M. Guardascione, H. P. Spaink, C. Doglioni, B. E. Snaar-Jagalska, M. Santarosa, R. Maestro, Cell Death Differ. 2018, 12, 2165.
- D. K. Patten, G. Corleone, B. Gyorffy, Y. Perone, N. Slaven, I. Barozzi, E. Erdos, A. Saiakhova, K. Goddard, A. Vingiani, S. Shousha, L. S. Pongor, D. J. Hadjiminas, G. Schiavon, P. Barry, C. Palmieri, R. C. Coombes, P. Scacheri, G. Pruneri, L. Magnani, Nat. Med. 2018, 9, 1469.
- L. Zhang, J. Qiang, X. Yang, D. Wang, A. U. Rehman, X. He, W. Chen, D. Sheng, L. Zhou, Y. Z. Jiang, T. Li, Y. Du, J. Feng, X. Hu, J. Zhang, X. C. Hu, Z. M. Shao, S. Liu, Adv. Sci. (Weinh) 2020, 1, 1901728.
- Y. Qin, Y. Hou, S. Liu, P. Zhu, X. Wan, M. Zhao, M. Peng, H. Zeng, Q. Li, T. Jin, X. Cui, M. Liu, Adv. Sci. (Weinh) 2021, 2, 2002232.
- F. Yang, Z. He, H. Duan, D. Zhang, J. Li, H. Yang, J. F. Dorsey, W. Zou, S. A. Nabavizadeh, S. J. Bagley, K. Abdullah, S. Brem, L. Zhang, X. Xu, K. T. Byrne, R. H. Vonderheide, Y. Gong, Y. Fan, Nat. Commun. 2021, 1, 3424.
- J. Shi, W. Gao, F. Shao, Trends Biochem. Sci. 2017, 4, 245.
- S. K. Vanaja, V. A. Rathinam, K. A. Fitzgerald, Trends Cell Biol. 2015, 5, 308.
- H. I. Muendlein, W. M. Connolly, Z. Magri, I. Smirnova, V. Ilyukha, A. Gautam, A. Degterev, A. Poltorak, Nat. Commun. 2021, 1, 86.
- E. S. Weiss, C. Girard-Guyonvarc'h, D. Holzinger, A. A. de Jesus, Z. Tariq, J. Picarsic, E. J. Schiffrin, D. Foell, A. A. Grom, S. Ammann, S. Ehl, T. Hoshino, R. Goldbach-Mansky, C. Gabay, S. W. Canna, Blood 2018, 13, 1442.
- R. Loveless, R. Bloomquist, Y. Teng, J Exp Clin Cancer Res 2021, 1, 264.
- J. Ding, K. Wang, W. Liu, Y. She, Q. Sun, J. Shi, H. Sun, D. C. Wang, F. Shao, Nature 2016, 7610, 111.
- J. Ruan, S. Xia, X. Liu, J. Lieberman, H. Wu, Nature 2018, 7703, 62.
- J. Shi, Y. Zhao, K. Wang, X. Shi, Y. Wang, H. Huang, Y. Zhuang, T. Cai, F. Wang, F. Shao, Nature 2015, 7575, 660.
- X. Chen, W. T. He, L. Hu, J. Li, Y. Fang, X. Wang, X. Xu, Z. Wang, K. Huang, J. Han, Cell Res. 2016, 9, 1007.
- A. Bobrie, M. Colombo, G. Raposo, C. Thery, Traffic 2011, 12, 1659.
- R. Kalluri, V. S. LeBleu, Science 2020, 367, 6478.
- L. Mashouri, H. Yousefi, A. R. Aref, A. M. Ahadi, F. Molaei, S. K. Alahari, Mol Cancer 2019, 1, 75.
- G. Kim, Y. Lee, J. Ha, S. Han, M. Lee, J Control Release 2021, 330, 684.
- C. P. Lai, E. Y. Kim, C. E. Badr, R. Weissleder, T. R. Mempel, B. A. Tannous, X. O. Breakefield, Nat. Commun. 2015, 6, 7029.
- A. Mizrak, M. F. Bolukbasi, G. B. Ozdener, G. J. Brenner, S. Madlener, E. P. Erkan, T. Strobel, X. O. Breakefield, O. Saydam, Mol. Ther. 2013, 1, 101.
- Y. Tian, S. Li, J. Song, T. Ji, M. Zhu, G. J. Anderson, J. Wei, G. Nie, Biomaterials 2014, 7, 2383.
- Q. Ou-Yang, B. Yan, A. Li, Z. S. Hu, J. N. Feng, X. X. Lun, M. M. Zhang, M. D. Zhang, K. C. Wu, F. F. Xue, A. G. Yang, J. Zhao, Biomaterials 2018, 178, 170.
- Q. Wang, Y. Wang, J. Ding, C. Wang, X. Zhou, W. Gao, H. Huang, F. Shao, Z. Liu, Nature 2020, 7799, 421.
- Y. Wang, W. Gao, X. Shi, J. Ding, W. Liu, H. He, K. Wang, F. Shao, Nature 2017, 7661, 99.
- J. Hou, R. Zhao, W. Xia, C. W. Chang, Y. You, J. M. Hsu, L. Nie, Y. Chen, Y. C. Wang, C. Liu, W. J. Wang, Y. Wu, B. Ke, J. L. Hsu, K. Huang, Z. Ye, Y. Yang, X. Xia, Y. Li, C. W. Li, B. Shao, J. A. Tainer, M. C. Hung, Nat. Cell Biol. 2020, 10, 1264.
- F. Humphries, L. Shmuel-Galia, N. Ketelut-Carneiro, S. Li, B. Wang, V. V. Nemmara, R. Wilson, Z. Jiang, F. Khalighinejad, K. Muneeruddin, S. A. Shaffer, R. Dutta, C. Ionete, S. Pesiridis, S. Yang, P. R. Thompson, K. A. Fitzgerald, Science 2020, 6511, 1633.
- J. Y. Zhang, B. Zhou, R. Y. Sun, Y. L. Ai, K. Cheng, F. N. Li, B. R. Wang, F. J. Liu, Z. H. Jiang, W. J. Wang, D. Zhou, H. Z. Chen, Q. Wu, Cell Res. 2021, 9, 980.
- Z. Zhang, Y. Zhang, S. Xia, Q. Kong, S. Li, X. Liu, C. Junqueira, K. F. Meza-Sosa, T. M. Y. Mok, J. Ansara, S. Sengupta, Y. Yao, H. Wu, J. Lieberman, Nature 2020, 7799, 415.
- N. Kayagaki, I. B. Stowe, B. L. Lee, K. O'Rourke, K. Anderson, S. Warming, T. Cuellar, B. Haley, M. Roose-Girma, Q. T. Phung, P. S. Liu, J. R. Lill, H. Li, J. Wu, S. Kummerfeld, J. Zhang, W. P. Lee, S. J. Snipas, G. S. Salvesen, L. X. Morris, L. Fitzgerald, Y. Zhang, E. M. Bertram, C. C. Goodnow, V. M. Dixit, Nature 2015, 7575, 666.
- R. Kojima, D. Bojar, G. Rizzi, G. C. Hamri, M. D. El-Baba, P. Saxena, S. Auslander, K. R. Tan, M. Fussenegger, Nat. Commun. 2018, 1, 1305.
- Z. Li, X. Zhou, X. Gao, D. Bai, Y. Dong, W. Sun, L. Zhao, M. Wei, X. Yang, G. Yang, L. Yuan, J Extracell Vesicles 2020, 1, 1816710.
- Z. Fu, X. Zhang, X. Zhou, U. Ur-Rehman, M. Yu, H. Liang, H. Guo, X. Guo, Y. Kong, Y. Su, Y. Ye, X. Hu, W. Cheng, J. Wu, Y. Wang, Y. Gu, S. F. Lu, D. Wu, K. Zen, J. Li, C. Yan, C. Y. Zhang, X. Chen, Cell Res. 2021, 6, 631.
- S. Tasaki, J. Xu, D. R. Avey, L. Johnson, V. A. Petyuk, R. J. Dawe, D. A. Bennett, Y. Wang, C. Gaiteri, Nat. Commun. 2022, 1, 655.
- T. Saleh, W. Jankowski, G. Sriram, P. Rossi, S. Shah, K. B. Lee, L. A. Cruz, A. J. Rodriguez, R. B. Birge, C. G. Kalodimos, Nat. Chem. Biol. 2016, 2, 117.
- H. J. Kim, S. Ogura, T. Otabe, R. Kamegawa, M. Sato, K. Kataoka, K. Miyata, ACS Cent. Sci. 2019, 11, 1866.
- K. Josephson, A. Ricardo, J. W. Szostak, Drug Discov Today 2014, 4, 388.
- D. Mateju, B. Eichenberger, F. Voigt, J. Eglinger, G. Roth, J. A. Chao, Cell 2020, 7, 1801.
- D. Wang, H. Wu, S. Z. F. Phua, G. Yang, W. Qi Lim, L. Gu, C. Qian, H. Wang, Z. Guo, H. Chen, Y. Zhao, Nat. Commun. 2020, 1, 357.
- Y. Wang, N. Gong, C. Ma, Y. Zhang, H. Tan, G. Qing, J. Zhang, Y. Wang, J. Wang, S. Chen, X. Li, Q. Ni, Y. Yuan, Y. Gan, J. Chen, F. Li, J. Zhang, C. Ou, Y. Zhao, X. Liu, X. J. Liang, Nat. Commun. 2021, 1, 4964.
- Q. Yin, A. Pan, B. Chen, Z. Wang, M. Tang, Y. Yan, Y. Wang, H. Xia, W. Chen, H. Du, M. Chen, C. Fu, Y. Wang, X. Yuan, Z. Lu, Q. Zhang, Y. Wang, Nat. Commun. 2021, 1, 2385.
- D. S. Chen, I. Mellman, Immunity 2013, 1, 1.
- L. Huang, Y. Rong, X. Tang, K. Yi, P. Qi, J. Hou, W. Liu, Y. He, X. Gao, C. Yuan, F. Wang, Mol Cancer 2022, 1, 45.
- G. T. Motz, G. Coukos, Immunity 2013, 1, 61.
- J. Nam, S. Son, L. J. Ochyl, R. Kuai, A. Schwendeman, J. J. Moon, Nat. Commun. 2018, 1, 1074.
- D. M. Pardoll, Nat. Rev. Cancer 2012, 4, 252.
- T. Wang, S. Cai, M. Wang, W. Zhang, K. Zhang, D. Chen, Z. Li, S. Jiang, J. Med. Chem. 2021, 11, 7390.
- K. Aslan, V. Turco, J. Blobner, J. K. Sonner, A. R. Liuzzi, N. G. Nunez, D. De Feo, P. Kickingereder, M. Fischer, E. Green, A. Sadik, M. Friedrich, K. Sanghvi, M. Kilian, F. Cichon, L. Wolf, K. Jahne, A. von Landenberg, L. Bunse, F. Sahm, D. Schrimpf, J. Meyer, A. Alexander, G. Brugnara, R. Roth, K. Pfleiderer, B. Niesler, A. von Deimling, C. Opitz, M. O. Breckwoldt, et al., Nat. Commun. 2020, 1, 931.
- Z. Yang, Y. Zhu, Z. Dong, W. Li, N. Yang, X. Wang, L. Feng, Z. Liu, Nat. Commun. 2021, 1, 4299.
- P. Zhao, M. Wang, M. Chen, Z. Chen, X. Peng, F. Zhou, J. Song, J. Qu, Biomaterials 2020, 254, 120142.
Cited by
Sorted by citations
Recent advances in extracellular vesicles for therapeutic cargo delivery
Kim, H. I., Park, J. B., Zhu, Y., Wang, X., Han, Y., & Zhang, D. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01201-6 · Cited by 504 · see citing works
Zhang, M., Liu, C.-J., Tu, J., Tang, M., Ashrafizadeh, M., Nabavi, N., Sethi, G., Zhao, P., & Liu, S. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02305-x · Cited by 299 · see citing works
Exosome for mRNA delivery: Strategies and therapeutic applications
Iqbal, Z., Rehman, K., Mahmood, A., Shabbir, M., Liang, Y., Duan, L., & Zeng, H. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02634-x · Cited by 144 · see citing works
Hu, Y., Liu, Y., Zong, L., Zhang, W., Liu, R., Xing, Q., Liu, Z., Yan, Q., Li, W., Lei, H., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06382-y · Cited by 127 · see citing works
From structural design to delivery: mRNA therapeutics for cancer immunotherapy
Zhou, F., Huang, L., Li, S., Yang, W., Chen, F., Cai, Z., Liu, X., Xu, W., Lehto, V., Lächelt, U., et al. (2023) · Exploration · doi:10.1002/exp.20210146 · Cited by 115 · see citing works
Bahadorani, M., Nasiri, M., Dellinger, K., Aravamudhan, S., & Zadegan, R. M. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s464249 · Cited by 125 · see citing works
Clinical relevance of extracellular vesicles in cancer — therapeutic and diagnostic potential
Greening, D. W., Xu, R., Rai, A., Suwakulsiri, W., Chen, M., & Simpson, R. J. (2025) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-025-01074-2 · Cited by 114 · see citing works
Genetically engineered loaded extracellular vesicles for drug delivery
Erana-Perez, Z., Igartúa, M., Santos‐Vizcaíno, E., & Hernández, R. M. (2024) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2024.02.006 · Cited by 77 · see citing works
Extracellular vesicles as next generation immunotherapeutics
Greening, D. W., Xu, R., Ale, A., Hagemeyer, C. E., & Chen, W. (2023) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2023.02.002 · Cited by 61 · see citing works
Regulated cell death‐amplified sonodynamic anti‐tumor immune nanotherapeutics
Zhou, L., Chen, Y., Xie, D., Li, K., Cui, X., Dietrich, C. F., Nussler, A. K., & Zhang, X. (2024) · BMEMat · doi:10.1002/bmm2.12079 · Cited by 58 · see citing works
Cell Death Pathway Regulation by Functional Nanomedicines for Robust Antitumor Immunity
Li, Y., Guo, Y., Zhang, K., Zhu, R., Chen, X. S., Zhang, Z., & Yang, W. (2023) · Advanced Science · doi:10.1002/advs.202306580 · Cited by 51 · see citing works
Extracellular vesicles as carriers of mRNA: Opportunities and challenges in diagnosis and treatment
Kirian, R. D., Steinman, D., Jewell, C. M., & Zierden, H. C. (2024) · Theranostics · doi:10.7150/thno.93115 · Cited by 46 · see citing works
Lipid bilayer-based biological nanoplatforms for sonodynamic cancer therapy
Li, S., Mok, G. S. P., & Dai, Y. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115110 · Cited by 41 · see citing works
Pyroptosis: Induction and inhibition strategies for immunotherapy of diseases
Wu, J., Wang, H., Gao, P., & Ouyang, S. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.06.026 · Cited by 42 · see citing works
Extracellular Vesicle‐Based mRNA Therapeutics and Vaccines
Li, Q., Xing, H., Naeem, A., Zhang, K., Zheng, A., Huang, Y., & Lu, M. (2025) · Exploration · doi:10.1002/exp.20240109 · Cited by 42 · see citing works
Jing, Z., Huang, W., Mei, J., Bhushan, S., Wu, X., Yan, C., Zheng, H., & Yang, Y. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02445-0 · Cited by 40 · see citing works
Extracellular Vesicles: A New Star for Gene Drug Delivery
Sun, M., Zhang, H., Liu, J., Chen, J., Cui, Y., Wang, S., Zhang, X., & Yang, Z. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s446224 · Cited by 38 · see citing works
Zhao, R., Deng, X., Tang, Y., Yang, X., Ge, Z., Wang, D., Shen, Y., Jiang, L., Lin, W., Zheng, C., et al. (2024) · ACS Nano · doi:10.1021/acsnano.3c13102 · Cited by 30 · see citing works
Guo, X., Yang, Z., Guo, Z., Lai, H., Meng, H., Meng, M., Li, T., Li, Z., Chen, J., Feng, Y., et al. (2025) · Advanced Materials · doi:10.1002/adma.202410998 · Cited by 29 · see citing works
Extracellular Vesicle-Based Drug Delivery Systems in Cancer Therapy
Wu, J., Jin, Z., Fu, T., Yu, Q., Bian, X., Zhang, X., & Zhang, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104835 · Cited by 29 · see citing works
Xu, S., Qian, Z., Zhao, N., & Yuan, W. (2023) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2023.10.145 · Cited by 29 · see citing works
Recent Progress in Extracellular Vesicle-Based Carriers for Targeted Drug Delivery in Cancer Therapy
Tang, Y., Liu, X., Sun, M., Xiong, S., Xiao, N., Li, J., He, X., & Xie, J. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15071902 · Cited by 24 · see citing works
Huang, Y., Wang, C., Chen, Y., Wang, D., & Yao, D. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.05.021 · Cited by 24 · see citing works
Engineering materials for pyroptosis induction in cancer treatment
Liu, J., Chen, T., Liu, X., Li, Z., & Zhang, Y. (2023) · Bioactive Materials · doi:10.1016/j.bioactmat.2023.10.027 · Cited by 22 · see citing works
Nanomaterials Enhance Pyroptosis-Based Tumor Immunotherapy
Ji, F., Shi, C., Shu, Z., & Li, Z. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s457309 · Cited by 21 · see citing works
Engineering exosomes for mRNA delivery: a review
Yao, T. S., Dong, X., Wang, X., Liu, X., Fu, L., & Li, L. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.144662 · Cited by 23 · see citing works
Feng, L., Wu, Y., Yang, Y., Yue, B., Peng, C. Y., Chen, C., Fu, P., Du, J., & Long, F. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113070 · Cited by 19 · see citing works
Extracellular vesicles for breast cancer diagnosis and therapy
Shi, J., Zhang, H., Cui, Y., Xing, J., Wang, W., Chen, J., Wang, S., & Yang, Z. (2024) · Extracellular Vesicle · doi:10.1016/j.vesic.2024.100039 · Cited by 18 · see citing works
Xie, H., Liang, B., Zhu, Q., Wang, L., Li, H., Qin, Z., Zhang, J., Liu, Z., & Wu, Y. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116433 · Cited by 18 · see citing works
Igniting hope: Harnessing NLRP3 inflammasome-GSDMD-mediated pyroptosis for cancer immunotherapy
Li, L., Chen, L., & Sun, Z. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122951 · Cited by 18 · see citing works
Role of tumor cell pyroptosis in anti-tumor immunotherapy
Zhang, L., Bai, H., Zhou, J., Ye, L., & Gao, L. (2024) · Cell Insight · doi:10.1016/j.cellin.2024.100153 · Cited by 15 · see citing works
Novel immunotherapies for breast cancer: Focus on 2023 findings
Lan, H., Chen, M., Yao, S.-Y., Chen, J.-X., & Jin, K. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111549 · Cited by 14 · see citing works
Zhang, S., Liang, Y., Ji, P., Zheng, R., Fan, L., Hou, G., Yang, G., & Yuan, L. (2024) · Advanced Science · doi:10.1002/advs.202305891 · Cited by 14 · see citing works
Self-citationMei, C., Liu, Y., Liu, Z., Zhi, Y., Jiang, Z., Lyu, X., & Wang, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms26010145 · Cited by 14 · see citing works
Huang, Z., Wei, C., Chen, Y., Jiang, Q., Wang, Y.-Q., Wang, Y., Xu, T., Lü, N., Huang, Z., & Xu, X. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.12.061 · Cited by 14 · see citing works
Shuai, Y., Ma, Z., Ju, J., Li, C., Bai, X., Yue, J., Wang, X., Yuan, P., & Qian, H. (2024) · APOPTOSIS · doi:10.1007/s10495-024-02037-1 · Cited by 13 · see citing works
Zhen, X., Jia, L., Tang, Q., Zhao, Y., Li, P., Li, J., Xie, X., & Wang, S. (2023) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2023.05.114 · Cited by 12 · see citing works
Hu, Y., Yu, Q., Li, X., Wang, J., Guo, L., Huang, L., & Gao, W. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202403493 · Cited by 12 · see citing works
The role of extracellular vesicles in immune cell exhaustion and resistance to immunotherapy
Aghakhani, A., Pezeshki, P. S., & Rezaei, N. (2024) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2024.2360209 · Cited by 11 · see citing works
Insight into the structure, function and the tumor suppression effect of gasdermin E
Long, Y., Jia, X., & Chu, L. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116348 · Cited by 10 · see citing works
Light Triggered “Bacterial Bomb” to Amplify Tumor Pyroptosis
Liu, Y., Zeng, T., Bai, S.-Y., Fang, X., Cao, X.-P., Li, S.-Q., Chen, Q., Lu, C.-H., & Yang, H.-H. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202505784 · Cited by 13 · see citing works
Zhang, R., Xu, Z., Xu, S., Li, R., & Qian, H. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s550390 · Cited by 10 · see citing works
CD81-guided heterologous EVs present heterogeneous interactions with breast cancer cells
Gurrieri, E., Carradori, G., Roccuzzo, M., Pancher, M., Peroni, D., Belli, R., Trevisan, C., Notarangelo, M., Huang, W., Carreira, Á. S. A., et al. (2024) · Journal of Biomedical Science · doi:10.1186/s12929-024-01084-9 · Cited by 8 · see citing works
Regulation of gasdermins in pyroptosis and cytokine release
Li, S., Bracey, S., Liu, Z., & Xiao, T. S. (2023) · Advances in immunology · doi:10.1016/bs.ai.2023.03.002 · Cited by 8 · see citing works
Nanomaterials‐Induced Pyroptosis: Advancing Novel Therapeutic Pathways in Nanomedicine
Yu, S., Zhang, Y., Zhou, Z., Li, J., & Meng, H. (2025) · Small Methods · doi:10.1002/smtd.202401290 · Cited by 7 · see citing works
Gu, M. J., Chen, W., Ding, S., Lin, Z., Qian, L., Xiao, W., Jia, X., Lu, G., & Gong, W. (2025) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-025-04104-1 · Cited by 7 · see citing works
Extracellular vesicles in cancer: golden goose or Trojan horse
Han, T., Hao, Q., Chao, T., Sun, Q., Chen, Y., Gao, B., Guan, L., Ren, W., & Zhou, X. Y. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae025 · Cited by 6 · see citing works
Potential of Exosomes as Multifunctional Nanocarriers for Targeted Drug Delivery
Al-Ani, S. A., Lee, Q. Y., Maheswaran, D., Sin, Y. M., Loh, J. S., Foo, J. B., Hamzah, S. B., Ng, J. F., & Tan, L. (2024) · Molecular Biotechnology · doi:10.1007/s12033-024-01268-6 · Cited by 6 · see citing works
Shao, S., Chen, X., Chen, Y., Wang, M., Huang, J., Wang, J., Yu, X., Li, X., Zhang, Y., Yuan, P., et al. (2025) · 中国科学通报:英文版 · doi:10.1016/j.scib.2025.04.015 · Cited by 4 · see citing works
Exosomes from Cancer Cells: Innovative Approach for Targeted Cancer Treatment
Hosseinpouri, A., Saberi, M., Yazdansetad, Z., Arabpour, Z., & Zarei‐Behjani, Z. (2025) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-025-00393-1 · Cited by 4 · see citing works
Wei, J., Zheng, W., Teng, C., An, X., Li, L., Zhong, P., Peng, C., Zhuge, S., Ampadu, J. A., Yu, C., et al. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112311 · Cited by 4 · see citing works
Advanced extracellular vesicle immunotherapy
Zhang, J., Mu, Y., Ji, X., Jiang, X., Wang, R., Ding, X., & Wang, L. (2026) · FlexMat. · doi:10.1002/flm2.70030 · Cited by 3 · see citing works
Li, J., Cheng, H., & Liu, X. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1804877 · Cited by 3 · see citing works
Precision Engineering of Extracellular Vesicles as Programmable Carriers for mRNA Therapeutics
Yoon, H., Lee, G., Jo, J., Koo, J., Kim, E., Choi, H. J., Jung, S., Shin, Y., Oh, K. T., & Lim, C. (2026) · International Journal of Nanomedicine · doi:10.2147/ijn.s595161 · Cited by 3 · see citing works
Huang, L. J., Chen, F., Chen, L., Zhan, S. T., Liu, M. M., Xiang, J. D., Zhang, Q., & Yang, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1570901 · Cited by 2 · see citing works
NLRPs and tumor: research progress from molecular mechanisms to clinical applications
Song, L., Cao, Y., & Tao, Y. (2025) · Oncogene · doi:10.1038/s41388-025-03642-3 · Cited by 2 · see citing works
Nanotechnology-mediated precision delivery of mRNA
Deng, H., Li, L., Zhao, C., Wang, Z., Xiao, Y., Huang, P., Siegwart, D. J., & Chen, X. S. (2026) · Nature Materials · doi:10.1038/s41563-026-02623-5 · Cited by 2 · see citing works
Liu, M., Li, X., LIU, J., & Liu, Y. (2024) · Biocell · doi:10.32604/biocell.2024.053227 · Cited by 2 · see citing works
Sun, J., Li, T., Cui, J., Zhang, L., Wang, G., Ma, C., Zhang, C., & Wang, Y. (2025) · Oncogene · doi:10.1038/s41388-025-03356-6 · Cited by 2 · see citing works
Lu, W., Yu, S., Wang, L., Yao-Zhang, Ou, Q.-Q., Liu, Y.-C., & Yu, L. (2025) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukaryotgeneexpr.2025058852 · Cited by 1 · see citing works
Cancer-Immunity Cycle-Based Smart Nucleic Acid Nanodrugs for Potentiated Immunotherapy
Wu, B., Chen, J., Jiang, L., Zhao, Z., Shan, X., Ouyang, C., Jiang, P., Tong, X., Lü, Y., Zhang, J., et al. (2026) · ACS Nano Medicine · doi:10.1021/acsnanomed.5c00202 · Cited by 1 · see citing works
Tatiparthi, R., Panda, A., Chaitanya, M., Gashe, F., Hasan, G., & Yarlagadda, R. (2026) · Molecular Imaging and Biology · doi:10.1007/s11307-026-02090-z · Cited by 1 · see citing works
Nabeta, E., Wang, A., Zhao, J., & Hao, D. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27146121 · Cited by 1 · see citing works
Self-citationExtracellular vesicles for next-gen therapeutics and drug delivery
Khan, N., Ahmadova, Z., Shi, Y., Shafiq, T., Liang, Y., & Duan, L. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00571-9 · Cited by 1 · see citing works
Xie, H., Liang, B., Zhu, Q., Wang, L., Li, H., Qin, Z., Zhang, J., Liu, Z., & Wu, Y. (2024) · Research Square · doi:10.21203/rs.3.rs-3844462/v1
Extracellular vesicles the delivery of drugs through genetic engineering
Ankur, J., Soni, P., Malviya, N., Sapna, M., & Kharia, A. (2024) · International Journal of Pharmaceutical Chemistry and Analysis · doi:10.18231/j.ijpca.2024.017
Vesicular Systems for Anticancer Drug Delivery
Garanin, A., Плевако, Д. С., Васильева, О. А., & Malek, A. V. (2025) · Nanobiotechnology Reports · doi:10.1134/s2635167625600506
Li, W. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-11681-6
Salah, R. A., Shouman, S., Abouzid, A. E., Ehab, S., El-Qassas, J., Mohamed, A., & El‐Badri, N. (2026) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-032-12705-1_11
Extracellular vesicles in solid tumors: from tumor ecology to engineered therapeutics
Cai, W., Chen, Y., Dai, S., Cheng, C., & Chen, L. (2026) · Molecular Cancer · doi:10.1186/s12943-026-02705-7
Pyroptosis‐Inducing Nanomedicine for Cancer Immunotherapy: Mechanisms and Emerging Strategies
Wang, P., Sun, X., Yang, Y., Zhang, S., He, Z., Wang, Y., & Luo, C. (2026) · Advanced Healthcare Materials · doi:10.1002/adhm.71578
Role of pyroptosis in melanoma: Molecular mechanisms and therapeutic potentials
Zhang, X.-H., Zhang, K., Qu, X.-C., Zhang, J., Laila, U. E., Wang, B., Si, W.-R., Jiang, Q., & Wu, D.-D. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02403-1
Zhang, Q., Wei, T., Lan, Z., Lin, G., Xu, M., Li, X., & Bao, Y. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1988247
Engineered extracellular vesicles as next-generation platforms for mRNA therapeutics delivery
Xiao, Y., Tong, X., Wang, Z., Zhang, Y., Liu, S., Tian, M., Chen, Y., Gan, L., Yang, X., & Yong, T. (2026) · Biomaterials Science · doi:10.1039/d6bm00986g
- Authors
- Xing, Y., Zhang, F., Ji, P., Wei, M., Yin, C., Yang, A., Yang, G., & Zhao, J.
- Affiliations
- Air Force Medical University (CN)
- Xijing Hospital (CN)
- Corresponding author
- Yang, Angang
- Yang, Guodong
- Zhao, Jing
- Venue
- Small
- Publisher
- Wiley
- Published
- 2023-01-12
- Volume
- 19
- Issue
- 20
- Pages
- e2204031-e2204031
- ISSN
- 1613-6810 (ISSN-L)
- 1613-6829
- OpenAlex
- W4315928852
- Cited by
- 74
- References
- 52
- Citations by year
- 2026: 15 · 2025: 19 · 2024: 30 · 2023: 10
- FWCI
- 6.59
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Small (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (81972871)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- pyroptosis, engineered extracellular vesicles, mRNA delivery, cancer immunotherapy, HER2-positive breast cancer, chlorin e6, sonodynamic therapy, antitumor immunity, tumor suppression
- MeSH terms
- Extracellular Vesicles, Pyroptosis, Animals, Disease Models, Animal, Immunotherapy, Intracellular Signaling Peptides and Proteins, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review