Evidence map›Paper›PMID 38437557›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Targeting and monitoring ovarian cancer invasion with an RNAi and peptide delivery system.

Liangliang Hao, Natalie Boehnke, Susanna K Elledge, Nour-Saïda Harzallah, Renee T Zhao, Eva Cai, Yu-Xiong Feng, Sofia Neaher, Heather E Fleming, Piyush B Gupta and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Clinical applications of oligonucleotides for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  5. Is Emerging Nanomedicine a Friend or Foe to Germ Cells?International journal of nanomedicine · 2025
    Review
  6. RNA delivery systems.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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

12 authors at 6 institutions in 1 country.

Liangliang Hao *Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-7513-3922
Natalie Boehnke *Department of Chemical Engineering and Materials Science, University of Minnesota Twin Cities, Minneapolis, MN 55455.ORCID 0000-0002-3468-2033
Susanna K Elledge *Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Nour-Saïda HarzallahKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0009-0008-3420-8391
Renee T ZhaoKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Eva CaiKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Yu-Xiong FengDepartment of Biology, Whitehead Institute for Biomedical Research, Cambridge, MA 02142.
Sofia NeaherKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0009-0001-8253-6874
Heather E FlemingKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0002-5286-3794
Piyush B GuptaNaveris, Waltham, MA 02451.
Paula T HammondKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Sangeeta N BhatiaKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.ORCID 0000-0001-6525-101X
Massachusetts Institute of Technology · USHarvard University · USBroad Institute · USInstitute for Soldier Nanotechnologies · USUniversity of Minnesota · USWhitehead Institute for Biomedical Research · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Jacqueline A. Lees · 1985 to 2026
$93.9M
TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI NILES, JACQUIN C · 1985 to 2020
$25.6M
Understanding drug delivery through an integrated barcoding approachK99CA255844 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOEHNKE, NATALIE · 2021 to 2022
$308k
Developing multiplexed microenvironmental sensors for precision diagnostics of cancer metastasisK99CA237861 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HAO, LIANGLIANG · 2020 to 2021
$203k
NCI NIH HHS K99 CA237861NCI NIH HHS K99 CA255844NCI NIH HHS P30 CA014051NIEHS NIH HHS P30 ES002109
6 · The paper itself

Abstract

RNA interference (RNAi) therapeutics are an emerging class of medicines that selectively target mRNA transcripts to silence protein production and combat disease. Despite the recent progress, a generalizable approach for monitoring the efficacy of RNAi therapeutics without invasive biopsy remains a challenge. Here, we describe the development of a self-reporting, theranostic nanoparticle that delivers siRNA to silence a protein that drives cancer progression while also monitoring the functional activity of its downstream targets. Our therapeutic target is the transcription factor SMARCE1, which was previously identified as a key driver of invasion in early-stage breast cancer. Using a doxycycline-inducible shRNA knockdown in OVCAR8 ovarian cancer cells both in vitro and in vivo, we demonstrate that SMARCE1 is a master regulator of genes encoding proinvasive proteases in a model of human ovarian cancer. We additionally map the peptide cleavage profiles of SMARCE1-regulated proteases so as to design a readout for downstream enzymatic activity. To demonstrate the therapeutic and diagnostic potential of our approach, we engineered self-assembled layer-by-layer nanoparticles that can encapsulate nucleic acid cargo and be decorated with peptide substrates that release a urinary reporter upon exposure to SMARCE1-related proteases. In an orthotopic ovarian cancer xenograft model, theranostic nanoparticles were able to knockdown SMARCE1 which was in turn reported through a reduction in protease-activated urinary reporters. These LBL nanoparticles both silence gene products by delivering siRNA and noninvasively report on downstream target activity by delivering synthetic biomarkers to sites of disease, enabling dose-finding studies as well as longitudinal assessments of efficacy.

Indexed as

Ovarian NeoplasmsPeptidesChromosomal Proteins, Non-HistoneDNA-Binding ProteinsEndopeptidasesFemaleHumansPeptide HydrolasesRNA InterferenceRNA, Small InterferingChromosomal Proteins, Non-HistoneDNA-Binding ProteinsEndopeptidasesPeptide HydrolasesPeptidesRNA, Small InterferingSMARCE1 protein, humanLayer-by-layer assemblyproteasesRNAi deliverysynthetic biomarkertheranostics

Identifiers

PMID38437557
PMCPMC10945808
OpenAlexW4392383032

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.