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For: Taha EA, Ono K, Eguchi T. Roles of Extracellular HSPs as Biomarkers in Immune Surveillance and Immune Evasion. Int J Mol Sci 2019;20:E4588. [PMID: 31533245 DOI: 10.3390/ijms20184588] [Cited by in Crossref: 41] [Cited by in F6Publishing: 41] [Article Influence: 13.7] [Reference Citation Analysis]
Number Citing Articles
1 Masaud SM, Szasz O, Szasz AM, Ejaz H, Anwar RA, Szasz A. A Potential Bioelectromagnetic Method to Slow Down the Progression and Prevent the Development of Ultimate Pulmonary Fibrosis by COVID-19. Front Immunol 2020;11:556335. [PMID: 33343561 DOI: 10.3389/fimmu.2020.556335] [Reference Citation Analysis]
2 Li S, Yi M, Dong B, Jiao Y, Luo S, Wu K. The roles of exosomes in cancer drug resistance and its therapeutic application. Clin Transl Med 2020;10:e257. [PMID: 33377643 DOI: 10.1002/ctm2.257] [Cited by in Crossref: 2] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
3 Chen C, Wang YS, Zhang ET, Li GA, Liu WY, Li Y, Jin YH. (20S) Ginsenoside Rh2 Exerts Its Anti-Tumor Effect by Disrupting the HSP90A-Cdc37 System in Human Liver Cancer Cells. Int J Mol Sci 2021;22:13170. [PMID: 34884975 DOI: 10.3390/ijms222313170] [Reference Citation Analysis]
4 Okusha Y, Eguchi T, Tran MT, Sogawa C, Yoshida K, Itagaki M, Taha EA, Ono K, Aoyama E, Okamura H, Kozaki KI, Calderwood SK, Takigawa M, Okamoto K. Extracellular Vesicles Enriched with Moonlighting Metalloproteinase Are Highly Transmissive, Pro-Tumorigenic, and Trans-Activates Cellular Communication Network Factor (CCN2/CTGF): CRISPR against Cancer. Cancers (Basel) 2020;12:E881. [PMID: 32260433 DOI: 10.3390/cancers12040881] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
5 Schoedel K, Miller V, Osei-Hwedieh D, Watters R, Duensing A, John I, Chandran U, Chang A, Soman V, Weiss K. Differential expression of angiogenesis markers HSP70, HSP90, VEGF and pERK1/2 in both components of dedifferentiated chondrosarcomas. J Bone Oncol 2021;29:100370. [PMID: 34094840 DOI: 10.1016/j.jbo.2021.100370] [Reference Citation Analysis]
6 Dias ML, O'Connor KM, Dempsey EM, O'Halloran KD, McDonald FB. Targeting the Toll-like receptor pathway as a therapeutic strategy for neonatal infection. Am J Physiol Regul Integr Comp Physiol 2021;321:R879-902. [PMID: 34612068 DOI: 10.1152/ajpregu.00307.2020] [Reference Citation Analysis]
7 Jego G, Hermetet F, Girodon F, Garrido C. Chaperoning STAT3/5 by Heat Shock Proteins: Interest of Their Targeting in Cancer Therapy. Cancers (Basel) 2019;12:E21. [PMID: 31861612 DOI: 10.3390/cancers12010021] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
8 Chomova M. Toward the Decipherment of Molecular Interactions in the Diabetic Brain. Biomedicines 2022;10:115. [DOI: 10.3390/biomedicines10010115] [Reference Citation Analysis]
9 Lu Y, Eguchi T, Sogawa C, Taha EA, Tran MT, Nara T, Wei P, Fukuoka S, Miyawaki T, Okamoto K. Exosome-Based Molecular Transfer Activity of Macrophage-Like Cells Involves Viability of Oral Carcinoma Cells: Size Exclusion Chromatography and Concentration Filter Method. Cells 2021;10:1328. [PMID: 34071980 DOI: 10.3390/cells10061328] [Reference Citation Analysis]
10 Caporossi D, Parisi A, Fantini C, Grazioli E, Cerulli C, Dimauro I. AlphaB-crystallin and breast cancer: role and possible therapeutic strategies. Cell Stress Chaperones 2021;26:19-28. [PMID: 33111264 DOI: 10.1007/s12192-020-01175-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Taha EA, Sogawa C, Okusha Y, Kawai H, Oo MW, Elseoudi A, Lu Y, Nagatsuka H, Kubota S, Satoh A, Okamoto K, Eguchi T. Knockout of MMP3 Weakens Solid Tumor Organoids and Cancer Extracellular Vesicles. Cancers (Basel) 2020;12:E1260. [PMID: 32429403 DOI: 10.3390/cancers12051260] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
12 Zou J, Peng H, Liu Y. The Roles of Exosomes in Immunoregulation and Autoimmune Thyroid Diseases. Front Immunol 2021;12:757674. [PMID: 34867996 DOI: 10.3389/fimmu.2021.757674] [Reference Citation Analysis]
13 Lian P, Braber S, Varasteh S, Wichers HJ, Folkerts G. Hypoxia and heat stress affect epithelial integrity in a Caco-2/HT-29 co-culture. Sci Rep 2021;11:13186. [PMID: 34162953 DOI: 10.1038/s41598-021-92574-5] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Van den Broek B, Wuyts C, Irobi J. Extracellular vesicle-associated small heat shock proteins as therapeutic agents in neurodegenerative diseases and beyond. Adv Drug Deliv Rev 2021;179:114009. [PMID: 34673130 DOI: 10.1016/j.addr.2021.114009] [Reference Citation Analysis]
15 Li C, Chen YM. Endoplasmic Reticulum-Associated Biomarkers for Molecular Phenotyping of Rare Kidney Disease. Int J Mol Sci 2021;22:2161. [PMID: 33671535 DOI: 10.3390/ijms22042161] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
16 Jang GY, Lee JW, Kim YS, Lee SE, Han HD, Hong KJ, Kang TH, Park YM. Interactions between tumor-derived proteins and Toll-like receptors. Exp Mol Med 2020;52:1926-35. [PMID: 33299138 DOI: 10.1038/s12276-020-00540-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
17 Marozzi M, Parnigoni A, Negri A, Viola M, Vigetti D, Passi A, Karousou E, Rizzi F. Inflammation, Extracellular Matrix Remodeling, and Proteostasis in Tumor Microenvironment. Int J Mol Sci 2021;22:8102. [PMID: 34360868 DOI: 10.3390/ijms22158102] [Reference Citation Analysis]
18 Boliukh I, Rombel-Bryzek A, Żuk O, Radecka B. The role of heat shock proteins in neoplastic processes and the research on their importance in the diagnosis and treatment of cancer. Contemp Oncol (Pozn) 2021;25:73-9. [PMID: 34667432 DOI: 10.5114/wo.2021.106006] [Reference Citation Analysis]
19 de Lima Filho JB, Freire L, Nahas EAP, Orsatti FL, Orsatti CL. Heat Shock Protein 60 Antibodies Are Associated With a Risk Factor for Cardiovascular Disease in Bedridden Elderly Patients. Front Mol Biosci 2020;7:103. [PMID: 32613007 DOI: 10.3389/fmolb.2020.00103] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
20 Jafari A, Rezaei-Tavirani M, Farhadihosseinabadi B, Taranejoo S, Zali H. HSP90 and Co-chaperones: Impact on Tumor Progression and Prospects for Molecular-Targeted Cancer Therapy. Cancer Invest 2020;38:310-28. [PMID: 32274949 DOI: 10.1080/07357907.2020.1752227] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 5.0] [Reference Citation Analysis]
21 Tomiyama E, Matsuzaki K, Fujita K, Shiromizu T, Narumi R, Jingushi K, Koh Y, Matsushita M, Nakano K, Hayashi Y, Wang C, Ishizuya Y, Kato T, Hatano K, Kawashima A, Ujike T, Uemura M, Takao T, Adachi J, Tomonaga T, Nonomura N. Proteomic analysis of urinary and tissue-exudative extracellular vesicles to discover novel bladder cancer biomarkers. Cancer Sci 2021;112:2033-45. [PMID: 33721374 DOI: 10.1111/cas.14881] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
22 Eguchi T, Sheta M, Fujii M, Calderwood SK. Cancer extracellular vesicles, tumoroid models, and tumor microenvironment. Semin Cancer Biol 2022:S1044-579X(22)00003-7. [PMID: 35032650 DOI: 10.1016/j.semcancer.2022.01.003] [Reference Citation Analysis]
23 Feng K, Ma R, Zhang L, Li H, Tang Y, Du G, Niu D, Yin D. The Role of Exosomes in Thyroid Cancer and Their Potential Clinical Application. Front Oncol 2020;10:596132. [PMID: 33335859 DOI: 10.3389/fonc.2020.596132] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
24 Prince TL, Lang BJ, Guerrero-Gimenez ME, Fernandez-Muñoz JM, Ackerman A, Calderwood SK. HSF1: Primary Factor in Molecular Chaperone Expression and a Major Contributor to Cancer Morbidity. Cells 2020;9:E1046. [PMID: 32331382 DOI: 10.3390/cells9041046] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
25 López-Martín E, Jorge-Barreiro FJ, Relova-Quintero JL, Salas-Sánchez AA, Ares-Pena FJ. Exposure to 2.45 GHz radiofrequency modulates calcitonin-dependent activity and HSP-90 protein in parafollicular cells of rat thyroid gland. Tissue Cell 2021;68:101478. [PMID: 33373917 DOI: 10.1016/j.tice.2020.101478] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
26 Sun Y, Zhang Y, Ren S, Li X, Yang P, Zhu J, Lin L, Wang Z, Jia Y. Low expression of RGL4 is associated with a poor prognosis and immune infiltration in lung adenocarcinoma patients. Int Immunopharmacol 2020;83:106454. [PMID: 32259700 DOI: 10.1016/j.intimp.2020.106454] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Aranda-Anzaldo A, Dent MAR. Is cancer a disease set up by cellular stress responses? Cell Stress Chaperones 2021;26:597-609. [PMID: 34031811 DOI: 10.1007/s12192-021-01214-4] [Reference Citation Analysis]
28 Zhao R, Zhao T, He Z, Cai R, Pang W. Composition, isolation, identification and function of adipose tissue-derived exosomes. Adipocyte 2021;10:587-604. [PMID: 34709975 DOI: 10.1080/21623945.2021.1983242] [Reference Citation Analysis]
29 Yang S, Xiao H, Cao L. Recent advances in heat shock proteins in cancer diagnosis, prognosis, metabolism and treatment. Biomed Pharmacother 2021;142:112074. [PMID: 34426258 DOI: 10.1016/j.biopha.2021.112074] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
30 Eguchi T, Taha EA, Calderwood SK, Ono K. A Novel Model of Cancer Drug Resistance: Oncosomal Release of Cytotoxic and Antibody-Based Drugs. Biology (Basel) 2020;9:E47. [PMID: 32150875 DOI: 10.3390/biology9030047] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
31 Khalyfa A, Sanz-Rubio D. The Mystery of Red Blood Cells Extracellular Vesicles in Sleep Apnea with Metabolic Dysfunction. Int J Mol Sci 2021;22:4301. [PMID: 33919065 DOI: 10.3390/ijms22094301] [Reference Citation Analysis]
32 Alharbi MG, Lee SH, Abdelazim AM, Saadeldin IM, Abomughaid MM. Role of Extracellular Vesicles in Compromising Cellular Resilience to Environmental Stressors. Biomed Res Int 2021;2021:9912281. [PMID: 34337063 DOI: 10.1155/2021/9912281] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Liyanagamage DSNK, Martinus RD. Role of Mitochondrial Stress Protein HSP60 in Diabetes-Induced Neuroinflammation. Mediators Inflamm 2020;2020:8073516. [PMID: 32410865 DOI: 10.1155/2020/8073516] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
34 Ono K, Sogawa C, Kawai H, Tran MT, Taha EA, Lu Y, Oo MW, Okusha Y, Okamura H, Ibaragi S, Takigawa M, Kozaki KI, Nagatsuka H, Sasaki A, Okamoto K, Calderwood SK, Eguchi T. Triple knockdown of CDC37, HSP90-alpha and HSP90-beta diminishes extracellular vesicles-driven malignancy events and macrophage M2 polarization in oral cancer. J Extracell Vesicles 2020;9:1769373. [PMID: 33144925 DOI: 10.1080/20013078.2020.1769373] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 6.5] [Reference Citation Analysis]
35 Caruso Bavisotto C, Marino Gammazza A, Campanella C, Bucchieri F, Cappello F. Extracellular heat shock proteins in cancer: From early diagnosis to new therapeutic approach. Semin Cancer Biol 2021:S1044-579X(21)00244-3. [PMID: 34563652 DOI: 10.1016/j.semcancer.2021.09.010] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 Gurunathan S, Kang MH, Qasim M, Khan K, Kim JH. Biogenesis, Membrane Trafficking, Functions, and Next Generation Nanotherapeutics Medicine of Extracellular Vesicles. Int J Nanomedicine 2021;16:3357-83. [PMID: 34040369 DOI: 10.2147/IJN.S310357] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
37 Androvitsanea A, Stylianou K, Drosataki E, Petrakis I. The Pathophysiological Role of Heat Shock Response in Autoimmunity: A Literature Review. Cells 2021;10:2626. [PMID: 34685607 DOI: 10.3390/cells10102626] [Reference Citation Analysis]
38 Purvinsh L, Gorshkov A, Brodskaia A, Vasin A. Extracellular Vesicles in Viral Pathogenesis: A Case of Dr. Jekyll and Mr. Hyde. Life (Basel) 2021;11:45. [PMID: 33450847 DOI: 10.3390/life11010045] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
39 Gerdtsson AS, Setayesh SM, Malihi PD, Ruiz C, Carlsson A, Nevarez R, Matsumoto N, Gerdtsson E, Zurita A, Logothetis C, Corn PG, Aparicio AM, Hicks J, Kuhn P. Large Extracellular Vesicle Characterization and Association with Circulating Tumor Cells in Metastatic Castrate Resistant Prostate Cancer. Cancers (Basel) 2021;13:1056. [PMID: 33801459 DOI: 10.3390/cancers13051056] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
40 Regimbeau M, Abrey J, Vautrot V, Causse S, Gobbo J, Garrido C. Heat shock proteins and exosomes in cancer theranostics. Semin Cancer Biol 2021:S1044-579X(21)00209-1. [PMID: 34343652 DOI: 10.1016/j.semcancer.2021.07.014] [Reference Citation Analysis]
41 Rodríguez-Vega A, Losada-Barragán M, Berbert LR, Mesquita-Rodrigues C, Bombaça ACS, Menna-Barreto R, Aquino P, Carvalho PC, Padrón G, de Jesus JB, Cuervo P. Quantitative analysis of proteins secreted by Leishmania (Viannia) braziliensis strains associated to distinct clinical manifestations of American Tegumentary Leishmaniasis. J Proteomics 2021;232:104077. [PMID: 33309930 DOI: 10.1016/j.jprot.2020.104077] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
42 Abu N, Rus Bakarurraini NAA, Nasir SN. Extracellular Vesicles and DAMPs in Cancer: A Mini-Review. Front Immunol 2021;12:740548. [PMID: 34721407 DOI: 10.3389/fimmu.2021.740548] [Reference Citation Analysis]
43 Oyama S, Yamamoto T, Yamayoshi A. Recent Advances in the Delivery Carriers and Chemical Conjugation Strategies for Nucleic Acid Drugs. Cancers (Basel) 2021;13:3881. [PMID: 34359781 DOI: 10.3390/cancers13153881] [Reference Citation Analysis]
44 De Almeida S, Regimbeau M, Jego G, Garrido C, Girodon F, Hermetet F. Heat Shock Proteins and PD-1/PD-L1 as Potential Therapeutic Targets in Myeloproliferative Neoplasms. Cancers (Basel) 2020;12:E2592. [PMID: 32932806 DOI: 10.3390/cancers12092592] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
45 Zhang R, Peng X, Lin J, Zhang Y, Zhan L, Tian X, Yin J, Zhao G. The Role of SREC-Ⅰ in Innate Immunity to Aspergillus fumigatus Keratitis. Invest Ophthalmol Vis Sci 2021;62:12. [PMID: 34236384 DOI: 10.1167/iovs.62.9.12] [Reference Citation Analysis]
46 Eguchi T, Sogawa C, Ono K, Matsumoto M, Tran MT, Okusha Y, Lang BJ, Okamoto K, Calderwood SK. Cell Stress Induced Stressome Release Including Damaged Membrane Vesicles and Extracellular HSP90 by Prostate Cancer Cells. Cells 2020;9:E755. [PMID: 32204513 DOI: 10.3390/cells9030755] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 6.5] [Reference Citation Analysis]
47 Zhao H, Raines LN, Huang SC. Molecular Chaperones: Molecular Assembly Line Brings Metabolism and Immunity in Shape. Metabolites 2020;10:E394. [PMID: 33023034 DOI: 10.3390/metabo10100394] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
48 Arda H, Doğanlar O. Stress-induced miRNAs isolated from wheat have a unique therapeutic potential in ultraviolet-stressed human keratinocyte cells. Environ Sci Pollut Res Int 2021. [PMID: 34677776 DOI: 10.1007/s11356-021-17039-8] [Reference Citation Analysis]
49 Seclì L, Fusella F, Avalle L, Brancaccio M. The dark-side of the outside: how extracellular heat shock proteins promote cancer. Cell Mol Life Sci 2021;78:4069-83. [PMID: 33544155 DOI: 10.1007/s00018-021-03764-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]