Evidence map›Paper›PMID 35163777›Full record

ReviewInternational journal of molecular sciences2022

Nanomedicine Strategies for Management of Drug Resistance in Lung Cancer.

Mohamed Haider, Amr Elsherbeny, Valeria Pittalà, Valeria Consoli, Maha Ali Alghamdi, Zahid Hussain, Ghalia Khoder, Khaled Greish

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% of its field
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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

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  12. Current Advances in Nanocarriers for Cancer Therapy.International journal of nanomedicine · 2025
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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

8 authors at 5 institutions in 5 countries.

Mohamed HaiderDepartment of Pharmaceutics and Pharmaceutical Technology, College of Pharmacy, University of Sharjah, Sharjah 27272, United Arab Emirates.ORCID 0000-0003-3150-9275
Amr ElsherbenyDivision of Molecular Therapeutics and Formulation, School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0003-0437-4299
Valeria PittalàDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0003-1856-0308
Valeria ConsoliDepartment of Drug and Health Science, University of Catania, 95125 Catania, Italy.ORCID 0000-0001-8961-5818
Maha Ali AlghamdiDepartment of Biotechnology, College of Science, Taif University, Taif 21974, Saudi Arabia.ORCID 0000-0002-5424-388X
Zahid HussainDepartment of Pharmaceutics and Pharmaceutical Technology, College of Pharmacy, University of Sharjah, Sharjah 27272, United Arab Emirates.ORCID 0000-0002-6978-3133
Ghalia KhoderDepartment of Pharmaceutics and Pharmaceutical Technology, College of Pharmacy, University of Sharjah, Sharjah 27272, United Arab Emirates.ORCID 0000-0002-6036-1022
Khaled GreishDepartment of Molecular Medicine, Princess Al-Jawhara Centre for Molecular Medicine, School of Medicine and Medical Sciences, Arabian Gulf University, Manama 329, Bahrain.ORCID 0000-0002-0787-7070
University of Sharjah · AEUniversity of Catania · ITArabian Gulf University · BHTaif University · SAUniversity of Nottingham · GB

Funding

Arabian Gulf University E002-PI-04/18University of Sharjah 2101110345
6 · The paper itself

Abstract

Lung cancer (LC) is one of the leading causes of cancer occurrence and mortality worldwide. Treatment of patients with advanced and metastatic LC presents a significant challenge, as malignant cells use different mechanisms to resist chemotherapy. Drug resistance (DR) is a complex process that occurs due to a variety of genetic and acquired factors. Identifying the mechanisms underlying DR in LC patients and possible therapeutic alternatives for more efficient therapy is a central goal of LC research. Advances in nanotechnology resulted in the development of targeted and multifunctional nanoscale drug constructs. The possible modulation of the components of nanomedicine, their surface functionalization, and the encapsulation of various active therapeutics provide promising tools to bypass crucial biological barriers. These attributes enhance the delivery of multiple therapeutic agents directly to the tumor microenvironment (TME), resulting in reversal of LC resistance to anticancer treatment. This review provides a broad framework for understanding the different molecular mechanisms of DR in lung cancer, presents novel nanomedicine therapeutics aimed at improving the efficacy of treatment of various forms of resistant LC; outlines current challenges in using nanotechnology for reversing DR; and discusses the future directions for the clinical application of nanomedicine in the management of LC resistance.

Indexed as

Antineoplastic AgentsDrug Delivery SystemsDrug Resistance, MultipleDrug Resistance, NeoplasmHumansLung NeoplasmsTheranostic NanomedicineTumor MicroenvironmentAntineoplastic Agentschemotherapeutic agentsdrug deliverydrug resistancelung cancernanomedicine

Identifiers

PMID35163777
PMCPMC8836587
OpenAlexW4220779294

What OpenQuestion 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 OpenQuestion graph.