4.5 Article

Pterostilbene enhances sorafenib's anticancer effects on gastric adenocarcinoma

Journal

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 24, Issue 21, Pages 12525-12536

Publisher

WILEY
DOI: 10.1111/jcmm.15795

Keywords

combination chemotherapy; gastric adenocarcinoma (GAC); pterostilbene; sorafenib; synergistic effect

Funding

  1. National Natural Science Foundation of China [81471964, 81772978, 81800647, 81972626]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_0048]
  3. CityU Applied Research [9667202]
  4. Jiangsu Provincial Special Program of Medical Science [BE2017611]
  5. Science and Technology Innovation Committee of Shenzhen Municipality [JCYJ20180507181627057, JCYJ20170818100531426]

Ask authors/readers for more resources

Sorafenib has been approved for the treatment of certain cancers in clinic. However, the effects of sorafenib on gastric adenocarcinoma (GAC) were still limited. This study aimed to evaluate both in vitro and in vivo efficacy of sorafenib in combination with pterostilbene (PTE) on the treatment of GAC. Here, the morphological changes and cell viability were recorded in both N87 and MKN45 cells. The cell cycle profile and apoptosis were assessed by flow cytometry. Subcutaneous tumour xenografts were constructed in nude mice, and IHC staining of the dissected tumour tissues was conducted. Our results showed that PTE enhanced sorafenib's inhibitory effects on cell viability. The obvious down-regulation of cyclin D1, Cdk-2, Cdk-4, Cdk-6 and p62 and the up-regulation of LC3II, caspase-9, caspase-3 and PARP cleavages were observed for the combination treatment with PTE and sorafenib than monotherapy. The combination treatment resulted in a higher level of cell cycle arrest at G1 phase and apoptosis than either drug. Besides, drug combination significantly enhanced the inhibition of tumour growth than sorafenib or PET alone in nude mice. The percentage of Ki-67- and PCNA-positive cells was distinctly reduced, and the apoptotic cells was obviously increased when compared with single drug therapy. Altogether, PET obviously enhanced sorafenib's antitumour effects against GAC through inhibiting cell proliferation, inducing autophagy and promoting apoptosis. The combination therapy with PET and sorafenib may serve as a novel therapeutic strategy for treating GAC and deserve further clinical trials.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biochemical Research Methods

The Glomerulus Multiomics Analysis Provides Deeper Insights into Diabetic Nephropathy

Tingting Zhao, Fang Cheng, Dongdong Zhan, Jin'e Li, Chunxia Zheng, Yinghui Lu, Weisong Qin, Zhihong Liu

Summary: By integrating the transcriptomics and proteomics profiles of DN patients and controls, researchers identified differentially expressed genes, constructed a regulatory network of transcription factors-target genes, and discovered new DN-specific proteins. This study provides deeper insights into the pathogenesis of DN and opens the potential avenue for finding new therapeutic interventions.

JOURNAL OF PROTEOME RESEARCH (2023)

Article Chemistry, Multidisciplinary

Near-infrared-activated anticancer platinum(IV) complexes directly photooxidize biomolecules in an oxygen-independent manner

Zhiqin Deng, Huangcan Li, Shu Chen, Na Wang, Gongyuan Liu, Danjun Liu, Weihui Ou, Feijie Xu, Xiong Wang, Dangyuan Lei, Pui-Chi Lo, Yang Yang Li, Jian Lu, Mengsu Yang, Ming-Liang He, Guangyu Zhu

Summary: This study reports the use of near-infrared-activated small-molecule Pt(IV) photooxidants to directly oxidize intracellular biomolecules. These photooxidants can effectively eliminate cancer stem cells and show low toxicity in the dark. Metal-enhanced photooxidation induced by these Pt(IV) complexes leads to robust photooxidation of survival-related biomolecules, inducing oxidative stress, disrupting intracellular pH (pHi) homeostasis, and initiating nonclassical necrosis.

NATURE CHEMISTRY (2023)

Article Neurosciences

Complement C4-deficient mice have a high mortality rate during PTZ-induced epileptic seizures, which correlates with cognitive problems and the deficiency in the expression of Egr1 and other immediate early genes

Tatyana Veremeyko, Rongcai Jiang, Mingliang He, Eugene D. Ponomarev

Summary: The complement system plays an important role in immune defense and also has important functions in the central nervous system (CNS). Recent studies have shown that complement subunits C1q, C4, and C3 have roles in synapse pruning and neurologic pathologies. C4B deficiency or low expression is related to the development of schizophrenia and autism spectrum disorders through mechanisms not related to synapse elimination. C4B has a role in the regulation of immediate early gene expression and downstream targets during CNS insults such as epileptic seizures.

FRONTIERS IN CELLULAR NEUROSCIENCE (2023)

Article Multidisciplinary Sciences

Mitochondrial ATP synthase as a direct molecular target of chromium(III) to ameliorate hyperglycaemia stress

Haibo Wang, Ligang Hu, Hongyan Li, Yau-Tsz Lai, Xueying Wei, Xiaohan Xu, Zhenkun Cao, Huiming Cao, Qianya Wan, Yuen-Yan Chang, Aimin Xu, Qunfang Zhou, Guibin Jiang, Ming-Liang He, Hongzhe Sun

Summary: In this study, the researchers identified the Cr(III)-proteome in cells and found that ATP synthase plays a crucial role in relieving hyperglycemia stress.

NATURE COMMUNICATIONS (2023)

Article Medicine, General & Internal

Genome-wide CRISPR/Cas9 screening identifies a targetable MEST-PURA interaction in cancer metastasis

Wen Wen, Long Liao, Wei Dai, Can-Can Zheng, Xiang-Peng Tan, Yan He, Qi-Hua Zhang, Zhi-Hao Huang, Wen-You Chen, Yan-Ru Qin, Kui-Sheng Chen, Ming-Liang He, Simon Law, Maria Li Lung, Qing-Yu He, Bin Li

Summary: Through genome-wide CRISPR/Cas9 screening and gene profiling, the MEST-PURA-SRCIN1/RASAL1-ERK-snail signaling cascade was identified as an important mechanism underlying cancer metastasis in esophageal squamous cell carcinoma. Blocking the interaction between MEST and PURA could be a potential therapeutic approach for managing tumor metastasis.

EBIOMEDICINE (2023)

Review Pharmacology & Pharmacy

Microneedles: An Emerging Vaccine Delivery Tool and a Prospective Solution to the Challenges of SARS-CoV-2 Mass Vaccination

Ya-Xiu Feng, Huan Hu, Yu-Yuen Wong, Xi Yao, Ming-Liang He

Summary: Vaccination is effective in preventing infectious diseases, and microneedles are a promising tool for painless vaccine delivery, with the advantage of avoiding cold chain storage and improving accessibility for special populations.

PHARMACEUTICS (2023)

Article Environmental Sciences

Dysregulation of MiR-199a/IL8 pathway in chronic Cr (VI)-induced tumor growth and angiogenesis

Lin Wang, Zhi-Hao Zhou, Yun-Xia Xie, Wen-Jing Liu, Rui-Xiang Zhang, Nan Jiang, Ming-Liang He, Jian-Ge Qiu, Bing-Hua Jiang

Summary: This study revealed the mechanism of Cr(VI) in inducing carcinogenesis and angiogenesis. Chronic exposure to Cr(VI) resulted in a significant decrease in miR-199a expression levels, while overexpression of miR-199a inhibited angiogenesis and tumor growth. Additionally, Cr(VI) exposure also resulted in an increase in CXCL8 levels, while overexpression of miR-199a suppressed CXCL8 expression. These results indicate that the miR-199a/IL8 pathway plays an important role in Cr(VI)-induced carcinogenesis and angiogenesis.

ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY (2023)

Review Biochemistry & Molecular Biology

The transcriptional regulators of virulence for Pseudomonas aeruginosa: Therapeutic opportunity and preventive potential of its clinical infections

Xiaolong Shao, Chunyan Yao, Yiqing Ding, Haiyan Hu, Guoliang Qian, Mingliang He, Xin Deng

Summary: In Pseudomonas aeruginosa, transcription factors play a crucial role in the genetic regulation of adaptability and pathogenicity. Several techniques have been used to identify TF binding sites on the P. aeruginosa genome, and an atlas of TF binding patterns has been created. This review summarizes recent literature on TF regulatory networks involved in various processes, including quorum sensing, biofilm formation, pyocyanin synthesis, motility, secretion systems, and oxidative stress responses. Insights from the global regulatory network of transcriptional regulators could inform strategies for preventing clinical infections caused by P. aeruginosa.

GENES & DISEASES (2023)

Review Biochemistry & Molecular Biology

Targeting Type I Interferon Induction and Signaling: How Zika Virus Escapes from Host Innate Immunity

Huan Hu, Yaxiu Feng, Ming-Liang He

Summary: Zika virus (ZIKV) infection causes neurological disorders and elicits a wide range of immune response. Type I interferons (IFNs) and its signaling cascade play a crucial role in innate immunity against ZIKV infection, but ZIKV can antagonize them. Toll-like receptors 3 (TLR3), TLR7/8 and RIG-I-like receptor 1 (RIG-1) recognize the ZIKV genome and induce the expression of Type I IFNs and interferon-stimulated genes (ISGs). ISGs exert antiviral activity at different stages of the ZIKV life cycle. The NS proteins of ZIKV directly interact with factors in the pathways to evade innate immunity, while structural proteins and antibody-binding of BDCA2 or inflammasome activation enhance ZIKV replication. In this review, recent findings about the interaction between ZIKV infection and type I IFNs pathways are summarized, and potential strategies for antiviral drug development are suggested.

INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES (2023)

Article Cell Biology

microRNA-497 slows esophageal cancer development and reverses chemotherapy resistance through its target QKI

Yun-Xia Xie, Zhi-Hao Zhou, Shu-Wen Liu, Ye Zhang, Wen-Jing Liu, Rui-Ke Zhang, Ming-Liang He, Jian-Ge Qiu, Lin Wang, Bing-Hua Jiang

Summary: This study showed that miR-497 is down-regulated in esophageal cancer and overexpression of miR-497 inhibits cell proliferation, tube formation, and migration. It was found that miR-497 directly binds to QKI and suppresses its expression. Overexpression of miR-497 also enhances the effect of chemotherapy and suppresses tumor growth in esophageal cancer in vivo.

AGING-US (2023)

Review Biochemistry & Molecular Biology

Metabolic alterations upon SARS-CoV-2 infection and potential therapeutic targets against coronavirus infection

Peiran Chen, Mandi Wu, Yaqing He, Binghua Jiang, Ming-Liang He

Summary: The COVID-19 pandemic caused by SARS-CoV-2 has brought enormous burden with high mortality rates. Targeting the interaction between SARS-CoV-2 and host metabolism holds promise for developing therapeutic strategies. This review summarizes recent studies on the role of host metabolism during the life cycle of SARS-CoV-2, with an emphasis on glucose and lipid metabolism, and discusses microbiota and long COVID-19. Repurposed metabolism-modulating drugs for COVID-19 are also discussed, including statins, ASM inhibitors, NSAIDs, Montelukast, omega-3 fatty acids, 2-DG, and metformin.

SIGNAL TRANSDUCTION AND TARGETED THERAPY (2023)

Article Biochemistry & Molecular Biology

Secreted LRPAP1 binds and triggers IFNAR1 degradation to facilitate virus evasion from cellular innate immunity

Huangcan Li, Xiong Wang, Yiran Wang, Yichen Li, Ying Chen, Yin-Ting Wong, Jufang He, Ming-Liang He

Summary: The proteases of SARS-CoV-2 and EV71 upregulate the expression and secretion of LRPAP1, which binds with IFNAR1 to trigger receptor degradation and enhance viral infection. A peptide derived from LRPAP1 can cause IFNAR1 degradation and enhance viral infections, while an LRPAP1 inhibitor stabilizes IFNAR1 and arrests virus infections. This study reveals a novel mechanism used by viruses to evade host immunity and provides a potential strategy for developing pan-antiviral drugs.

SIGNAL TRANSDUCTION AND TARGETED THERAPY (2023)

Article Medicine, Research & Experimental

Outbreak control management: Lessons from SARS-CoV-2 infections in 2020-2022 in Hong Kong, an international municipality with high-frequency travelers

Yaxiu Feng, Ching Han Young, Siu Hin Lau, Ming-Liang He

Summary: Control management of SARS-CoV-2 infections is a major challenge in the 21st century. While the government responded rapidly in the early days of the outbreak and achieved encouraging results, the high infectivity, new variants, and shortcomings in transmission control measures led to an uncontrollable outbreak in 2022. Vulnerable groups such as the elderly and children experienced high hospitalization and mortality rates due to low vaccination rates. This study timely summarizes the challenges, policies, and lessons learned from the SARS-CoV-2 outbreak from 2020 to 2022, providing valuable insights for other cities facing highly infectious SARS-CoV-2 outbreaks.

MEDCOMM (2022)

Article Biochemistry & Molecular Biology

Targeting m6A modification inhibits herpes virus 1 infection

Zhuoying Feng, Fanghang Zhou, Miaomiao Tan, Tingting Wang, Ying Chen, Wenwen Xu, Bin Li, Xin Wang, Xin Deng, Ming-Liang He

Summary: HSV-1 infection enhances the expression of m6A modification-related genes to facilitate viral replication, while inhibiting m6A modification reduces viral replication and reproduction.

GENES & DISEASES (2022)

Article Biochemistry & Molecular Biology

Ovarian Cancer Metastasis

Yichen Li, Qian Zhang, Mandi Wu, Peidong Zhang, Liang Huang, Xiaolin Ai, Zhengnan Yang, Qiuhong Shen, Yiran Wang, Ping Wang, Shengtao Zhou, Ming-Liang He

Summary: A study has found that a LncRNA associated with ovarian cancer metastasis, LncOVM, is highly correlated with poor prognosis and survival. LncOVM interacts with and stabilizes PPIP5K2, promoting the secretion of complement C5 from ovarian cancer cells, which then attracts myeloid-derived suppressor cells (MDSCs) infiltration in the tumor microenvironment (TME) to facilitate metastasis. Targeting the LncOVM-PPIP5K2-complement axis can inhibit MDSC infiltration and restore the suppression of tumorigenesis and metastasis.

INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES (2022)

No Data Available