Evidence map›Paper›PMID 34999182›Full record

ReviewPharmacology & therapeutics2022

Challenges and opportunities in metastatic breast cancer treatments: Nano-drug combinations delivered preferentially to metastatic cells may enhance therapeutic response.

Jesse Yu, Qingxin Mu, Millie Fung, Xiaolin Xu, Linxi Zhu, Rodney J Y Ho

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. [Preparation of HLYVSPW peptide-displaying outer membrane vesicles and validation of their in vitro targeting effects on triple-negative breast cancer cells].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2026
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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

6 authors at 1 institution in 1 country.

Jesse YuDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA.
Qingxin MuDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA.
Millie FungDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA.
Xiaolin XuDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA.
Linxi ZhuDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA.
Rodney J Y HoDepartment of Pharmaceutics, University of Washington, Seattle, WA 98195, USA; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA. Electronic address: rodneyho@uw.edu.
University of Washington · US

Funding

Targeted Long-acting Combination Antiretroviral Therapy (TLC-ART)UM1AI120176 · NIAID · UNIVERSITY OF WASHINGTON · PI COLLIER, ANN CORNWALL, HO, RODNEY J.Y. · 2015 to 2019
$15.0M
Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6M
NextGen Long-acting and targeted combination ART for Children with HIVR33AI149665 · NIAID · UNIVERSITY OF WASHINGTON · PI HO, RODNEY J.Y. · 2022 to 2025
$4.1M
NextGen Long-acting and targeted combination ART for Children with HIVR61AI149665 · NIAID · UNIVERSITY OF WASHINGTON · PI HO, RODNEY J.Y., MELVIN, ANN JORNS · 2020 to 2021
$2.1M
"NextGen Long-acting Platform: Targeted Combination Antiretrovirals"U01AI148055 · NIAID · UNIVERSITY OF WASHINGTON · PI BENDER IGNACIO, RACHEL ANN, HO, RODNEY J.Y. · 2019 to 2022
$1.6M
NIAID NIH HHS R33 AI149665NIAID NIH HHS R61 AI149665NIAID NIH HHS U01 AI148055NIAID NIH HHS UM1 AI120176NIGMS NIH HHS T32 GM007750
6 · The paper itself

Abstract

Despite advances in breast cancer treatments and related 5-year survival outcomes, metastatic breast cancer cures remain elusive. The current standard of care includes a combination of surgery, radiation therapy and drug therapy. However, even the most advanced procedures and treatments do not prevent breast cancer recurrence and metastasis. Once metastasis occurs, patient prognosis is poor. Recent elucidation of the spatiotemporal transit of metastatic cancer cells from primary tumor sites to distant sites provide an opportunity to integrate knowledge of drug disposition in our effort to enhance drug localization and exposure in cancer laden tissues . Novel technologies have been developed, but could be further refined to facilitate the distribution of drugs to target cancer cells and tissues. The purpose of this review is to highlight the challenges in metastatic breast cancer treatment and focus on novel drug combination and nanotechnology approaches to overcome the challenges. With improved definition of metastatic tissue target, directed localization and retention of multiple, pharmacologically active drugs to tissues and cells of interest may overcome the limitations in breast cancer treatment that may lead to a cure for breast cancer.

Indexed as

Breast NeoplasmsNanoparticlesCell Line, TumorFemaleHumansNanotechnologyNeoplasm Recurrence, LocalCombination therapyDrug deliveryMetastatic breast cancerNanoparticlesTargeted therapy

Identifiers

PMID34999182
PMCPMC9256851
OpenAlexW4206275853

What OpenQuestion holds

Textmetadata
LicenceTDM
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.