Evidence map›Paper›PMID 27036008›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Reporter nanoparticle that monitors its anticancer efficacy in real time.

Ashish Kulkarni, Poornima Rao, Siva Natarajan, Aaron Goldman, Venkata S Sabbisetti, Yashika Khater, Navya Korimerla, Vineethkrishna Chandrasekar, Raghunath A Mashelkar, Shiladitya Sengupta

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Review
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  4. Holography Meets Theranostics: DFT/TDDFT Insights into Ru-NO@MInternational journal of molecular sciences · 2025
    Article
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  16. Stimuli-Responsive Polymeric Nanoplatforms for Cancer Therapy.Frontiers in bioengineering and biotechnology · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Ashish KulkarniLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115; ashishk@mit.edu ram@ncl.res.in shiladit@mit.edu.
Poornima RaoLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Siva NatarajanLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Aaron GoldmanLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Venkata S SabbisettiDivision of Renal (Kidney) Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Yashika KhaterLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Navya KorimerlaLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Vineethkrishna ChandrasekarLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115;
Raghunath A MashelkarNational Chemical Laboratory, Pune 411008, India; ashishk@mit.edu ram@ncl.res.in shiladit@mit.edu.
Shiladitya SenguptaLaboratory of Nanomedicine, Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Harvard Medical School, Boston, MA 02115; Division of Biomedical Engineering, Harvard Medical School, Boston, MA 02115; Dana Farber Cancer Institute, Boston, MA 02115 ashishk@mit.edu ram@ncl.res.in shiladit@mit.edu.

Funding

Multifunctional nanoparticles for targeting aberrant tumorigenic pathwaysR01CA135242 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SENGUPTA, SHILADITYA · 2010 to 2014
$1.8M
NCI NIH HHS R01 CA135242
6 · The paper itself

Abstract

The ability to monitor the efficacy of an anticancer treatment in real time can have a critical effect on the outcome. Currently, clinical readouts of efficacy rely on indirect or anatomic measurements, which occur over prolonged time scales postchemotherapy or postimmunotherapy and may not be concordant with the actual effect. Here we describe the biology-inspired engineering of a simple 2-in-1 reporter nanoparticle that not only delivers a cytotoxic or an immunotherapy payload to the tumor but also reports back on the efficacy in real time. The reporter nanoparticles are engineered from a novel two-staged stimuli-responsive polymeric material with an optimal ratio of an enzyme-cleavable drug or immunotherapy (effector elements) and a drug function-activatable reporter element. The spatiotemporally constrained delivery of the effector and the reporter elements in a single nanoparticle produces maximum signal enhancement due to the availability of the reporter element in the same cell as the drug, thereby effectively capturing the temporal apoptosis process. Using chemotherapy-sensitive and chemotherapy-resistant tumors in vivo, we show that the reporter nanoparticles can provide a real-time noninvasive readout of tumor response to chemotherapy. The reporter nanoparticle can also monitor the efficacy of immune checkpoint inhibition in melanoma. The self-reporting capability, for the first time to our knowledge, captures an anticancer nanoparticle in action in vivo.

Indexed as

AnimalsAntineoplastic AgentsApoptosisB7-H1 AntigenCaspase 3Cell Line, TumorCell SurvivalDrug CarriersDrug MonitoringDrug Resistance, NeoplasmEsterasesFemaleFluorescent DyesHumansImmunoglobulin GMaleAntineoplastic AgentsB7-H1 AntigenCaspase 3Drug CarriersEsterasesFluorescent DyesImmunoglobulin GOligopeptidesPaclitaxelpoly(isobutylene-alt-maleic acid)Polymerschemotherapyimmunotherapymonitoringnanoparticlereporter

Identifiers

PMID27036008
PMCPMC4839457

What OpenQuestion holds

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Registered trials

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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.