Evidence map›Paper›PMID 34589378›Full record

ArticleNanophotonics (Berlin, Germany)2021

Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer.

Tanmoy Saha, Jayanta Mondal, Sachin Khiste, Hrvoje Lusic, Zhang-Wei Hu, Ruparoshni Jayabalan, Kevin J Hodgetts, HaeLin Jang, Shiladitya Sengupta, Somin Eunice Lee and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nanophotonics (Berlin, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Tanmoy SahaDivision of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Jayanta MondalDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Sachin KhisteDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Hrvoje LusicDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Zhang-Wei HuDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Ruparoshni JayabalanDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Kevin J HodgettsDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
HaeLin JangDivision of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Shiladitya SenguptaDivision of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Somin Eunice LeeDepartment of Electrical & Computer Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Younggeun ParkDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Luke P LeeDivision of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Aaron GoldmanDivision of Engineering in Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0002-9129-1311
Harvard University · USBrigham and Women's Hospital · USUniversity of Michigan · US

Funding

Engineering personalized micro-tumor ecosystemsU01CA214411 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI KHADEMHOSSEINI, ALI, SENGUPTA, SHILADITYA · 2017 to 2021
$3.5M
Whitlockite nanoparticle-based immunotherapy for bone metastasisR01CA236702 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI JANG, HAE LIN, SENGUPTA, SHILADITYA · 2019 to 2023
$2.7M
3D printed muscle-bone organ implant for treating large injuriesR01AR073135 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DOKMECI, MEHMET REMZI, JANG, HAE LIN · 2018 to 2022
$2.2M
Spatiotemporal delivery of synergistic drug combinations to kidney cancerR01CA229772 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SABBISETTI, VENKATA · 2018 to 2022
$1.9M
NCI NIH HHS R01 CA229772NCI NIH HHS R01 CA236702NCI NIH HHS U01 CA214411NIAMS NIH HHS R01 AR073135
6 · The paper itself

Abstract

Targeted delivery of drugs to tumor cells, which circumvent resistance mechanisms and induce cell killing, is a lingering challenge that requires innovative solutions. Here, we provide two bioengineered strategies in which nanotechnology is blended with cancer medicine to preferentially target distinct mechanisms of drug resistance. In the first 'case study', we demonstrate the use of lipid-drug conjugates that target molecular signaling pathways, which result from taxane-induced drug tolerance via cell surface lipid raft accumulations. Through a small molecule drug screen, we identify a kinase inhibitor that optimally destroys drug tolerant cancer cells and conjugate it to a rationally-chosen lipid scaffold, which enhances anticancer efficacy

Indexed as

cancer biologychemotherapydrug resistancenanomedicine

Identifiers

PMID34589378
PMCPMC8478290
OpenAlexW3173438130

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.