Evidence map›Paper›PMID 36153528›Full record

ReviewJournal of nanobiotechnology2022

Emerging nanotechnology-based therapeutics to combat multidrug-resistant cancer.

Priya Yadav, Suresh V Ambudkar, N Rajendra Prasad

Abstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Priya YadavDepartment of Biochemistry and Biotechnology, Annamalai University, Annamalainagar, Tamil Nadu, 608 002, India. priyayadav87@gmail.com.ORCID https://orcid.org/0000-0002-3627-6258
Suresh V AmbudkarLaboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 37 Convent Drive, Bethesda, MD, 20892-4256, USA. ambudkar@mail.nih.gov.ORCID https://orcid.org/0000-0002-2639-4955
N Rajendra PrasadDepartment of Biochemistry and Biotechnology, Annamalai University, Annamalainagar, Tamil Nadu, 608 002, India. drprasadnr@gmail.com.ORCID https://orcid.org/0000-0002-3937-8735

Funding

D. S. Kothari Postdoctoral Fellowship DSKPDF: No.F.4-2/2006 (BSR)/BL/20-21/0085)
6 · The paper itself

Abstract

Cancer often develops multidrug resistance (MDR) when cancer cells become resistant to numerous structurally and functionally different chemotherapeutic agents. MDR is considered one of the principal reasons for the failure of many forms of clinical chemotherapy. Several factors are involved in the development of MDR including increased expression of efflux transporters, the tumor microenvironment, changes in molecular targets and the activity of cancer stem cells. Recently, researchers have designed and developed a number of small molecule inhibitors and derivatives of natural compounds to overcome various mechanisms of clinical MDR. Unfortunately, most of the chemosensitizing approaches have failed in clinical trials due to non-specific interactions and adverse side effects at pharmacologically effective concentrations. Nanomedicine approaches provide an efficient drug delivery platform to overcome the limitations of conventional chemotherapy and improve therapeutic effectiveness. Multifunctional nanomaterials have been found to facilitate drug delivery by improving bioavailability and pharmacokinetics, enhancing the therapeutic efficacy of chemotherapeutic drugs to overcome MDR. In this review article, we discuss the major factors contributing to MDR and the limitations of existing chemotherapy- and nanocarrier-based drug delivery systems to overcome clinical MDR mechanisms. We critically review recent nanotechnology-based approaches to combat tumor heterogeneity, drug efflux mechanisms, DNA repair and apoptotic machineries to overcome clinical MDR. Recent successful therapies of this nature include liposomal nanoformulations, cRGDY-PEG-Cy5.5-Carbon dots and Cds/ZnS core-shell quantum dots that have been employed for the effective treatment of various cancer sub-types including small cell lung, head and neck and breast cancers.

Indexed as

Antineoplastic AgentsNeoplasmsCarbonDrug Resistance, MultipleDrug Resistance, NeoplasmHumansNanotechnologyTumor MicroenvironmentAntineoplastic AgentsCarbonABC transporterCancer stem cellsCombinational therapyDrug deliveryMultidrug resistanceNanotechnologyP-glycoproteinTumor microenvironment

Identifiers

PMID36153528
PMCPMC9509578

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.