Evidence map›Paper›PMID 36513723›Full record

ArticleScientific reports2022

Design of combination therapy for engineered bacterial therapeutics in non-small cell lung cancer.

Dhruba Deb, Yangfan Wu, Courtney Coker, Tetsuhiro Harimoto, Ruoqi Huang, Tal Danino

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Toward development of soil-derivedBiodesign research · 2026
    Article
  2. Microbial medicines: Unlocking the therapeutic potential of the microbiome in cancer treatment.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Review
  3. Review
  4. Review
  5. Designing live bacterial therapeutics for cancer.Advanced drug delivery reviews · 2025
    Review
  6. Review
  7. Article
  8. Bacterial live therapeutics for human diseases.Molecular systems biology · 2024
    Review
  9. Article
  10. Article
  11. 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

6 authors at 2 institutions in 1 country.

Dhruba DebDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Yangfan WuDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Courtney CokerDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Tetsuhiro HarimotoDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Ruoqi HuangDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA.
Tal DaninoDepartment of Biomedical Engineering, Columbia University, New York, NY, 10027, USA. tal.danino@columbia.edu.
Columbia University · USColumbia University Irving Medical Center · US

Funding

Engineering S. typhimurium for metastatic colorectal cancerR01EB029750 · NIBIB · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DANINO, TAL · 2020 to 2024
$1.4M
NIBIB NIH HHS R01 EB029750
6 · The paper itself

Abstract

Synthetic biology enables the engineering of bacteria to safely deliver potent payloads to tumors for effective anti-cancer therapies. However, a central challenge for translation is determining ideal bacterial therapy candidates for specific cancers and integrating them with other drug treatment strategies to maximize efficacy. To address this, we designed a screening and evaluation pipeline for characterization of bacterial therapies in lung cancer models. We screened 10 engineered bacterial toxins across 6 non-small cell lung cancer patient-derived cell lines and identified theta toxin as a promising therapeutic candidate. Using a bacteria-spheroid co-culture system (BSCC), analysis of differentially expressed transcripts and gene set enrichment revealed significant changes in at least 10 signaling pathways with bacteria-producing theta toxin. We assessed combinatorial treatment of small molecule pharmaceutical inhibitors targeting 5 signaling molecules and of 2 chemotherapy drugs along with bacterially-produced theta toxin and showed improved dose-dependent response. This combination strategy was further tested and confirmed, with AKT signaling as an example, in a mouse model of lung cancer. In summary, we developed a pipeline to rapidly characterize bacterial therapies and integrate them with current targeted therapies for lung cancer.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsAntineoplastic Combined Chemotherapy ProtocolsBacteriaCombined Modality TherapyMice

Identifiers

PMID36513723
PMCPMC9748036
OpenAlexW4311249532

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.