H3K27 acetylation activated‐CD109 evokes 5‐fluorouracil resistance in gastric cancer via the JNK/MAPK signaling pathway DOI Open Access
Fei Zhou, Leiming Wang, Han Ge

и другие.

Environmental Toxicology, Год журнала: 2023, Номер 38(12), С. 2857 - 2866

Опубликована: Сен. 4, 2023

Drug resistance is a considerable obstacle to gastric cancer (GC) treatment. The current work aimed elucidate the functional mechanism of CD109 in 5-fluorouracil (5-FU) GC. In this study, we demonstrated that was extremely heightened 5-FU-resistant GC cells. deficiency lessened IC50 value, impaired cell viability and metastatic capability, induced apoptosis after 5-FU treatment addition, found PAX5 bound p300 increased enrichment H3K27ac at promoter region gene, which resulted upregulation Moreover, also revealed triggered via activating JNK/MAPK signaling. Blockage signaling using JNK inhibitor, SP600125, abolished upregulation-induced changes values, viability, metastasis NCI-N87/5-FU SNU-1/5-FU Importantly, silencing enhanced therapeutic efficacy 5-FU, leading reduced tumor growth vivo. conclusion, our results unveiled H3K27 acetylation activated-CD109 cells modulating pathway, might provide an attractive target for

Язык: Английский

Extracellular vesicles and macrophages in tumor microenvironment: Impact on cervical cancer DOI Creative Commons

Wen Guo,

Wenqiong Liu, Junqing Wang

и другие.

Heliyon, Год журнала: 2024, Номер 10(15), С. e35063 - e35063

Опубликована: Июль 26, 2024

Язык: Английский

Процитировано

2

Magnolol’s Therapeutic Efficacy and Immunomodulatory Effects in Oral Squamous Cell Carcinoma DOI Open Access

Chien-Fu Tseng,

Hsin-Ming Chen,

Tsai-Lan Liao

и другие.

In Vivo, Год журнала: 2024, Номер 38(5), С. 2152 - 2164

Опубликована: Янв. 1, 2024

Oral squamous cell carcinoma (OSCC) presents a significant health challenge, requiring effective treatments. Magnolol, compound with potential anticancer properties, warrants investigation in OSCC treatment. Here, we aimed to assess the efficacy of magnolol inhibiting progression and explore underlying mechanisms its action.

Язык: Английский

Процитировано

1

Prostate cancer cell-derived exosomes ZNF667-AS1 reduces TGFBR1 mRNA stability to inhibit Treg expansion and DTX resistance by binding to U2AF1 DOI Creative Commons

Zhenfeng Shi,

Wenjing Pu,

Min Li

и другие.

Molecular Medicine, Год журнала: 2024, Номер 30(1)

Опубликована: Окт. 18, 2024

Docetaxel (DTX) resistance attenuates anti-tumor effects of DTX on prostate cancer (mCRPC) and drug was related to Treg expansion in tumors. ZNF667-AS1 played a suppressing role various tumors tumor-derived exosomes carry lncRNAs participate tumor progression. Here, the malignant characteristics PC effect its underlying molecular mechanism carrying were investigated.

Язык: Английский

Процитировано

1

Engineered exosomes in service of tumor immunotherapy: From optimizing tumor‐derived exosomes to delivering CRISPR/Cas9 system DOI
Mingyang Jiang, Ke Zhang,

Jinfeng Meng

и другие.

International Journal of Cancer, Год журнала: 2024, Номер 156(5), С. 898 - 913

Опубликована: Окт. 30, 2024

Exosomes can be modified and designed for various therapeutic goals because of their unique physical chemical characteristics. Researchers have identified tumor-derived exosomes (TEXs) as significant players in cancer by influencing tumor growth, immune response evasion, angiogeneis, drug resistance. TEXs promote the production specific proteins important progression. Due to easy accessibility, are being through genetic, delivery, membrane, system, alterations repurposed vehicles delivering drugs improve treatment outcomes. In complex vivo environment, clustered regularly interspaced short palindromic repeats CRISPR-associated protein 9 (CRISPR/Cas9) system encounters challenges from degradation, neutralization, responses, emphasizing need strategic distribution strategies effective genome editing. Engineered present a promising avenue CRISPR/Cas9 vivo. this review, we will explore different techniques enhancing using engineering strategies. Additionally, discuss how these incorporated into advanced genetic systems like possible uses.

Язык: Английский

Процитировано

1

Continued attention: The role of exosomal long non-coding RNAs in tumors over the past three years DOI Creative Commons

Jiarui Cao,

Bo Feng,

Yanchao Xv

и другие.

International Immunopharmacology, Год журнала: 2024, Номер 144, С. 113666 - 113666

Опубликована: Ноя. 21, 2024

Язык: Английский

Процитировано

1

H3K27 acetylation activated‐CD109 evokes 5‐fluorouracil resistance in gastric cancer via the JNK/MAPK signaling pathway DOI Open Access
Fei Zhou, Leiming Wang, Han Ge

и другие.

Environmental Toxicology, Год журнала: 2023, Номер 38(12), С. 2857 - 2866

Опубликована: Сен. 4, 2023

Drug resistance is a considerable obstacle to gastric cancer (GC) treatment. The current work aimed elucidate the functional mechanism of CD109 in 5-fluorouracil (5-FU) GC. In this study, we demonstrated that was extremely heightened 5-FU-resistant GC cells. deficiency lessened IC50 value, impaired cell viability and metastatic capability, induced apoptosis after 5-FU treatment addition, found PAX5 bound p300 increased enrichment H3K27ac at promoter region gene, which resulted upregulation Moreover, also revealed triggered via activating JNK/MAPK signaling. Blockage signaling using JNK inhibitor, SP600125, abolished upregulation-induced changes values, viability, metastasis NCI-N87/5-FU SNU-1/5-FU Importantly, silencing enhanced therapeutic efficacy 5-FU, leading reduced tumor growth vivo. conclusion, our results unveiled H3K27 acetylation activated-CD109 cells modulating pathway, might provide an attractive target for

Язык: Английский

Процитировано

3