Evidence map›Paper›PMID 34267368›Full record

ArticleNature materials2021

Microenvironment-triggered multimodal precision diagnostics.

Liangliang Hao, Nazanin Rohani, Renee T Zhao, Emilia M Pulver, Howard Mak, Olivia J Kelada, Henry Ko, Heather E Fleming, Frank B Gertler, Sangeeta N Bhatia

Open access · greenAbstract read
In one paragraph

Article in Nature materials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 70 citations in OpenAlex.

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  17. Exploration ofACS omega · 2023
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  19. A Cathepsin-Targeted Quenched Activity-Based Probe Facilitates Enhanced Detection of Human Tumors during Resection.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Liangliang HaoKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Nazanin RohaniKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Renee T ZhaoInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, USA.
Emilia M PulverInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, USA.
Howard MakKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Olivia J KeladaPreclinical Imaging, PerkinElmer, Hopkinton, MA, USA.ORCID http://orcid.org/0000-0003-1007-2801
Henry KoKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Heather E FlemingKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-5286-3794
Frank B GertlerKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Sangeeta N BhatiaKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA. sbhatia@mit.edu.ORCID http://orcid.org/0000-0002-1293-2097
Massachusetts Institute of Technology · USBroad Institute · USHoward Hughes Medical Institute · USPerkinElmer (United States) · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Paula T Hammond · 1985 to 2026
$93.9M
TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI YAFFE, MICHAEL B · 1985 to 2020
$25.6M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014051NIEHS NIH HHS P30 ES002109
6 · The paper itself

Abstract

Therapeutic outcomes in oncology may be aided by precision diagnostics that offer early detection, localization and the opportunity to monitor response to therapy. Here, we report a multimodal nanosensor engineered to target tumours through acidosis, respond to proteases in the microenvironment to release urinary reporters and (optionally) carry positron emission tomography probes to enable localization of primary and metastatic cancers in mouse models of colorectal cancer. We present a paradigm wherein this multimodal sensor can be employed longitudinally to assess burden of disease non-invasively, including tumour progression and response to chemotherapy. Specifically, we showed that acidosis-mediated tumour insertion enhanced on-target release of matrix metalloproteinase-responsive reporters in urine. Subsequent on-demand loading of the radiotracer

Indexed as

Multimodal ImagingPrecision MedicineTumor MicroenvironmentAcidosisAnimalsColorectal NeoplasmsDisease ProgressionFemaleFluorodeoxyglucose F18MiceMice, Inbred BALB CPositron-Emission TomographyFluorodeoxyglucose F18

Identifiers

PMID34267368
PMCPMC12341765
OpenAlexW3180194790

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.