Evidence map›Paper›PMID 30674994›Full record

ArticleCancer gene therapy2020

Enhanced noninvasive imaging of oncology models using the NIS reporter gene and bioluminescence imaging.

Rianna Vandergaast, Sarawut Khongwichit, Huailei Jiang, Timothy R DeGrado, Kah-Whye Peng, Duncan R Smith, Stephen J Russell, Lukkana Suksanpaisan

Open access · hybridAbstract read
In one paragraph

Article in Cancer gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Efficient radiolabeling of mesoporous silica nanoparticles for single-cell PET imaging.European journal of nuclear medicine and molecular imaging · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Development of a PromisingPharmaceuticals (Basel, Switzerland) · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Spatiotemporal PET Imaging Reveals Differences in CAR-T Tumor Retention in Triple-Negative Breast Cancer Models.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  12. Article
  13. How Non-invasiveFrontiers in physiology · 2020
    Review
  14. 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

8 authors at 4 institutions in 2 countries.

Rianna VandergaastImanis Life Sciences, Rochester, MN, 55902, USA.
Sarawut KhongwichitDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Huailei JiangDeparment of Radiology, Mayo Clinic, Rochester, MN, 55905, USA.
Timothy R DeGradoDeparment of Radiology, Mayo Clinic, Rochester, MN, 55905, USA.
Kah-Whye PengImanis Life Sciences, Rochester, MN, 55902, USA.
Duncan R SmithInstitute of Molecular Biosciences, Mahidol University, Salaya, Nakhon Pathom, 73170, Thailand.ORCID http://orcid.org/0000-0002-6592-9852
Stephen J RussellImanis Life Sciences, Rochester, MN, 55902, USA.
Lukkana SuksanpaisanImanis Life Sciences, Rochester, MN, 55902, USA. suksanpaisan@imanislife.com.
Mahidol University · THMayo Clinic · USMayo Clinic in Arizona · USMetLife (United States) · US

Funding

Phase 2: NIS proteins with altered anion specificityR44TR001191 · NCATS · IMANIS LIFE SCIENCES, LLC · PI RUSSELL, STEPHEN J, SUKSANPAISAN, LUKKANA · 2017 to 2018
$1.5M
NCATS NIH HHS R44 TR001191
6 · The paper itself

Abstract

Noninvasive bioluminescence imaging (BLI) of luciferase-expressing tumor cells has advanced pre-clinical evaluation of cancer therapies. Yet despite its successes, BLI is limited by poor spatial resolution and signal penetration, making it unusable for deep tissue or large animal imaging and preventing precise anatomical localization or signal quantification. To refine pre-clinical BLI methods and circumvent these limitations, we compared and ultimately combined BLI with tomographic, quantitative imaging of the sodium iodide symporter (NIS). To this end, we generated tumor cell lines expressing luciferase, NIS, or both reporters, and established tumor models in mice. BLI provided sensitive early detection of tumors and relatively easy monitoring of disease progression. However, spatial resolution was poor, and as the tumors grew, deep thoracic tumor signals were massked by overwhelming surface signals from superficial tumors. In contrast, NIS-expressing tumors were readily distinguished and precisely localized at all tissue depths by positron emission tomography (PET) or single photon emission computed tomography (SPECT) imaging. Furthermore, radiotracer uptake for each tumor could be quantitated noninvasively. Ultimately, combining BLI and NIS imaging represented a significant enhancement over traditional BLI, providing more information about tumor size and location. This combined imaging approach should facilitate comprehensive evaluation of tumor responses to given therapies.

Indexed as

AnimalsBenzothiazolesCell Line, TumorFemaleGenes, ReporterHumansLuciferases, FireflyLuminescent MeasurementsMiceMolecular ImagingNeoplasmsPositron-Emission TomographyRadiopharmaceuticalsSodium-Iodide SymportersSodium Pertechnetate Tc 99mSymportersBenzothiazolesD-luciferinLuciferases, FireflyRadiopharmaceuticalsSodium-Iodide SymportersSodium Pertechnetate Tc 99mSymporters

Identifiers

PMID30674994
PMCPMC7170803
OpenAlexW2911695507

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.