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混合纳米载体中使用植物化学物质和PARP抑制剂的联合疗法:结肠癌治疗的一种乐观方法

Combination Therapy Using Phytochemicals and PARP Inhibitors in Hybrid Nanocarriers: An Optimistic Approach for the Management of Colon Cancer.

作者信息

Qureshi Mohammad Javed, Narde Gurpreet Kaur, Ahuja Alka, Meenakshi Dhanalekshmi Unnikrishnan, Al Balushi Khalid

机构信息

Department of Pharmaceutics, College of Pharmacy, National University of Science and Technology, P.O. Box 620, Muscat PC130, Oman.

Department of Pharmacology and Biological Sciences, College of Pharmacy, National University of Science and Technology, P.O. Box 620, Muscat PC130, Oman.

出版信息

Int J Mol Sci. 2025 Jul 30;26(15):7350. doi: 10.3390/ijms26157350.


DOI:10.3390/ijms26157350
PMID:40806481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12347401/
Abstract

DNA damage repair is a hallmark of any cancer growth, eventually leading to drug resistance and death. The poly ADP-ribose polymerase (PARP) enzyme is vital in repairing damaged DNA in normal and cancer cells with mutated () genes. Inhibitors of the PARP enzyme aid in chemotherapy, as shown by drug combinations such as Olaparib and Irinotecan in breast cancer treatment. However, the effect of Olaparib in colon cancer has not been studied extensively. Synthetic drugs have a significant limitation in cancer treatment due to drug resistance, leading to colon cancer relapse. Bioavailability of Olaparib and other PARP inhibitors is limited due to their hydrophobicity, which poses a significant challenge. These limitations and challenges can be addressed by encapsulating Olaparib in nanoparticles that could possibly increase the bioavailability of the drug at the site of action. New age nanoparticles, such as hybrid nanoparticles, provide superior quality in terms of design and circulatory time of the drug in the plasma. The side effects of Olaparib as a chemotherapeutic pave the way for exploring phytochemicals that may have similar effects. The combined impact of Olaparib and phytochemicals such as genistein, resveratrol and others in nano-encapsulated form can be explored in the treatment of colon cancer.

摘要

DNA损伤修复是任何癌症生长的一个标志,最终会导致耐药性和死亡。聚ADP-核糖聚合酶(PARP)酶在修复正常细胞和携带突变()基因的癌细胞中的受损DNA方面至关重要。PARP酶抑制剂有助于化疗,如奥拉帕利和伊立替康联合用药在乳腺癌治疗中的效果所示。然而,奥拉帕利在结肠癌中的作用尚未得到广泛研究。由于耐药性,合成药物在癌症治疗中存在重大局限性,会导致结肠癌复发。奥拉帕利和其他PARP抑制剂因其疏水性,生物利用度有限,这构成了重大挑战。通过将奥拉帕利封装在纳米颗粒中可以解决这些局限性和挑战,这可能会提高药物在作用部位的生物利用度。新型纳米颗粒,如杂化纳米颗粒,在药物的设计和血浆循环时间方面具有卓越品质。奥拉帕利作为化疗药物的副作用为探索可能具有类似作用的植物化学物质铺平了道路。可以探索纳米封装形式的奥拉帕利与染料木黄酮、白藜芦醇等植物化学物质的联合作用在结肠癌治疗中的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/58dc835284ce/ijms-26-07350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/f1169e7beb25/ijms-26-07350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/4e1c37065dfd/ijms-26-07350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/cbb101469fc6/ijms-26-07350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/58dc835284ce/ijms-26-07350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/f1169e7beb25/ijms-26-07350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/4e1c37065dfd/ijms-26-07350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/cbb101469fc6/ijms-26-07350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7513/12347401/58dc835284ce/ijms-26-07350-g004.jpg

相似文献

[1]
Combination Therapy Using Phytochemicals and PARP Inhibitors in Hybrid Nanocarriers: An Optimistic Approach for the Management of Colon Cancer.

Int J Mol Sci. 2025-7-30

[2]
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[3]
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[4]
The Molecular Mechanisms of Actions, Effects, and Clinical Implications of PARP Inhibitors in Epithelial Ovarian Cancers: A Systematic Review.

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[5]
Olaparib Monotherapy or in Combination with Abiraterone for the Treatment of Patients with Metastatic Castration-Resistant Prostate Cancer (mCRPC) and a BRCA Mutation.

Target Oncol. 2025-5-21

[6]
The efficacy and safety of PARP inhibitors in mCRPC with HRR mutation in second-line treatment: a systematic review and bayesian network meta-analysis.

BMC Cancer. 2024-6-8

[7]
TP53 and DNA-PK as potential biomarkers for enhanced efficacy of Olaparib in colorectal cancer.

Invest New Drugs. 2025-5-16

[8]
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BMC Vet Res. 2025-7-5

[9]
Ivabradine induces RAD51 degradation, potentiating PARP inhibitor efficacy in non-germline BRCA pathogenic variant triple-negative breast cancer.

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[10]
Poly(ADP-ribose) polymerase (PARP) inhibitors for the treatment of ovarian cancer.

Cochrane Database Syst Rev. 2022-2-16

本文引用的文献

[1]
Assessing the antioxidant properties of Naringin and Rutin and investigating their oxidative DNA damage effects in breast cancer.

Sci Rep. 2024-7-3

[2]
Therapeutic Applications of Nanoformulated Resveratrol and Quercetin Phytochemicals in Colorectal Cancer-An Updated Review.

Pharmaceutics. 2024-6-4

[3]
Resveratrol and p53: How are they involved in CRC plasticity and apoptosis?

J Adv Res. 2024-12

[4]
Combination of Resveratrol and PARP inhibitor Olaparib efficiently deregulates homologous recombination repair pathway in breast cancer cells through inhibition of TIP60-mediated chromatin relaxation.

Med Oncol. 2024-1-6

[5]
Case Report: Progressive disease of BRCA2-mutant colon adenocarcinoma following talazoparib therapy.

Front Oncol. 2023-11-7

[6]
Lipid polymer hybrid nanoparticles: a custom-tailored next-generation approach for cancer therapeutics.

Mol Cancer. 2023-10-3

[7]
Lipid-Polymer Hybrid Nanosystems: A Rational Fusion for Advanced Therapeutic Delivery.

J Funct Biomater. 2023-8-23

[8]
Research progress on the anti-tumor effect of Naringin.

Front Pharmacol. 2023-8-17

[9]
Selection of potential natural compounds for poly-ADP-ribose polymerase (PARP) inhibition in glioblastoma therapy by in silico screening methods.

Saudi J Biol Sci. 2023-7

[10]
Treatment With Niraparib Maintenance Therapy in Patients With Newly Diagnosed Advanced Ovarian Cancer: A Phase 3 Randomized Clinical Trial.

JAMA Oncol. 2023-9-1

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