Prognostic value and gene regulatory network of CMSS1 in hepatocellular carcinoma DOI Creative Commons
Cheng Chen,

Caiming Wang,

Wei Liu

et al.

Cancer Biomarkers, Journal Year: 2023, Volume and Issue: 39(4), P. 361 - 370

Published: Dec. 29, 2023

Cms1 ribosomal small subunit homolog (CMSS1) is an RNA-binding protein that may play important role in tumorigenesis and development.

Language: Английский

Genetic and epigenetic defects of the RNA modification machinery in cancer DOI Creative Commons
Ines Oršolić,

Arnaud Carrier,

Manel Esteller

et al.

Trends in Genetics, Journal Year: 2022, Volume and Issue: 39(1), P. 74 - 88

Published: Nov. 12, 2022

Cancer was initially considered to be an exclusively genetic disease, but interplay of dysregulated and epigenetic mechanisms is now known contribute the cancer phenotype. More recently, chemical modifications RNA molecules - so-called epitranscriptome have been found regulate various aspects function homeostasis. Specific enzymes, as RNA-modifying proteins (RMPs), are responsible for depositing, removing, reading in RNA. Intensive investigations epitranscriptomic field recent years, conjunction with great technological advances, revealed critical role regulating numerous cellular pathways. Furthermore, growing evidence has that modification machinery often altered human cancers, highlighting enormous potential RMPs pharmacological targets or diagnostic markers.

Language: Английский

Citations

80

A bioinformatics analysis, pre-clinical and clinical conception of autophagy in pancreatic cancer: Complexity and simplicity in crosstalk DOI Creative Commons
Milad Ashrafizadeh, Wei Zhang, Rongjun Zou

et al.

Pharmacological Research, Journal Year: 2023, Volume and Issue: 194, P. 106822 - 106822

Published: June 17, 2023

Pancreatic cancer (PC) is a serious gastrointestinal tract disease for which the 5-year survival rate less than 10%, even in developed countries such as USA. The genomic profile alterations and dysregulated biological mechanisms commonly occur PC. Macroautophagy/autophagy cell death process that maintained at basal level physiological conditions, whereas its often changes during tumorigenesis. function of autophagy human cancers dual can be oncogenic onco-suppressor. Autophagy potent controller tumorigenesis supportive PC escalates growth cells suppression mediate death. also determines metastasis cells, it control EMT affecting migration. Moreover, starvation hypoxia stimulate glycolysis, glycolysis induction mediated by enhancing Furthermore, protective stimulates drug resistance gemcitabine inhibition enhance radiosensitivity. degrade MHC-I to immune evasion regulates polarization macrophages tumor microenvironment. Modulation activity provided silibinin, ursolic acid, chrysin huaier treatment Non-coding RNAs are controllers improve therapy response patients. mitophagy shows dysregulation PC, proliferation cells. Therefore, bioinformatics analysis demonstrates autophagy-related proteins genes biomarkers.

Language: Английский

Citations

65

Drug Resistance in Hepatocellular Carcinoma: Theoretical Basis and Therapeutic Aspects DOI Creative Commons

Ya-ruo Lei,

Xian-lu He,

Jun Li

et al.

Frontiers in Bioscience-Landmark, Journal Year: 2024, Volume and Issue: 29(2), P. 52 - 52

Published: Feb. 4, 2024

Primary liver cancer is one of the most common malignant tumors with high mortality and increasing incidence worldwide. Currently, chemotherapy an important comprehensive treatment for moderate or advanced cancer. Despite effective therapeutic effects initially achieved by chemotherapy, phenotypic molecular heterogeneity cells facilitates resistance to conventional targeted therapy even leads multidrug (MDR), which major obstacles clinical chemotherapy. Drug exhibits multiple complex mechanisms antagonize under pharmacological pressure, including overexpression drug efflux transporters, downstream adaptive response (such as apoptosis, autophagy, endoplasmic reticulum stress), dysfunction DNA damage repair (DDR), epigenetic modification, tumor microenvironment (TME) well extracellular matrix (ECM). In this paper, we summarize recent research progress intervention strategies in hepatocellular carcinoma (HCC), will provide a promising strategy overcoming MDR

Language: Английский

Citations

11

Targeting the “tumor microenvironment”: RNA-binding proteins in the spotlight in colorectal cancer therapy DOI
Yiwei Zhang, Yujun Zhang, Jingjing Song

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 131, P. 111876 - 111876

Published: March 16, 2024

Language: Английский

Citations

9

Dihydrotanshinone I targets ESR1 to induce DNA double-strand breaks and proliferation inhibition in hepatocellular carcinoma DOI

Yunmeng Nie,

Junbin Yan,

Xueru Huang

et al.

Phytomedicine, Journal Year: 2024, Volume and Issue: 130, P. 155767 - 155767

Published: May 24, 2024

Language: Английский

Citations

8

Fundamental insights and molecular interactions in pancreatic cancer: Pathways to therapeutic approaches DOI
Ming Gu, Yang Liu, Xin Peng

et al.

Cancer Letters, Journal Year: 2024, Volume and Issue: 588, P. 216738 - 216738

Published: Feb. 23, 2024

Language: Английский

Citations

7

Acquired and intrinsic gemcitabine resistance in pancreatic cancer therapy: Environmental factors, molecular profile and drug/nanotherapeutic approaches DOI Open Access
Milad Ashrafizadeh,

Kuo Luo,

Wei Zhang

et al.

Environmental Research, Journal Year: 2023, Volume and Issue: 240, P. 117443 - 117443

Published: Oct. 18, 2023

Language: Английский

Citations

15

Novel insights into mutual regulation between N6-methyladenosine modification and LncRNAs in tumors DOI Creative Commons
Nan Zhang, Yifei Sun, Zongqin Mei

et al.

Cancer Cell International, Journal Year: 2023, Volume and Issue: 23(1)

Published: June 26, 2023

Abstract N 6 -methyladenosine (m A), one of the most common RNA methylation modifications, has emerged in recent years as a new layer regulatory mechanism controlling gene expression eukaryotes. As reversible epigenetic modification, m A not only occurs on mRNAs but also Long non-coding RNAs (LncRNAs). we all known, despite LncRNAs cannot encode proteins, they affect proteins by interacting with or miRNAs, thus playing important roles occurrence and development variety tumors. Up to now, it been widely accepted that modification affects fate corresponding LncRNAs. Interestingly, levels functions modifications are mediated through affecting methyltransferases (METTL3, METTL14, WTAP, METTL16, etc.), demethylases (FTO, ALKBH5) methyl-binding (YTHDFs, YTHDCs, IGF2BPs, HNRNPs, which collectively referred “m regulators”. In this review, summarized mutual regulation mechanisms between cancer progression, metastasis, invasion drug resistance. detail, focus specific is demethylases, involves LncRNA first part. And section two intensively displays mediation via changing proteins. At last part, described interaction effects during various tumor development.

Language: Английский

Citations

14

The Emerging, Multifaceted Role of WTAP in Cancer and Cancer Therapeutics DOI Open Access

Guomin Ju,

Jiangchu Lei,

Shuqi Cai

et al.

Cancers, Journal Year: 2023, Volume and Issue: 15(11), P. 3053 - 3053

Published: June 4, 2023

Cancer is a grave and persistent illness, with the rates of both its occurrence death toll increasing at an alarming pace. N6-methyladenosine (m6A), most prevalent mRNA modification in eukaryotic organisms, catalyzed by methyltransferases has significant impact on various aspects cancer progression. WT1-associated protein (WTAP) crucial component m6A methyltransferase complex, catalyzing methylation RNA. It been demonstrated to participate numerous cellular pathophysiological processes, including X chromosome inactivation, cell proliferation, cycle regulation, alternative splicing. A better understanding role WTAP may render it reliable factor for early diagnosis prognosis, as well key therapeutic target treatment. found that closely related tumor metabolic autophagy, immunity, ferroptosis, epithelial mesenchymal transformation (EMT), drug resistance. In this review, we will focus latest advances biological functions cancer, explore prospects application clinical therapy.

Language: Английский

Citations

13

RNA-binding proteins in breast cancer: Biological implications and therapeutic opportunities DOI Creative Commons
Shimeng Wang,

Hexing Sun,

Guan‐Yuan Chen

et al.

Critical Reviews in Oncology/Hematology, Journal Year: 2024, Volume and Issue: 195, P. 104271 - 104271

Published: Jan. 23, 2024

RNA-binding proteins (RBPs) refer to a class of that participate in alternative splicing, RNA stability, polyadenylation, localization and translation RNAs, thus regulating gene expression post-transcriptional manner. Dysregulation RNA-RBP interaction contributes various diseases, including cancer. In breast cancer, disorders RBP function influence the biological characteristics tumor cells. Targeting RBPs has fostered development innovative therapies for However, RBP-related mechanisms cancer are not completely clear. this review, we summarize regulatory their signaling crosstalk Specifically, emphasize potential certain as prognostic factors due effects on proliferation, invasion, apoptosis, therapy resistance Most importantly, present comprehensive overview latest therapeutic strategies novel targets have proven be useful treatment

Language: Английский

Citations

4