Evidence map›Paper›PMID 39660610›Full record

ArticleCurrent protocols2024

In Vivo Bioluminescence Imaging of Tumor Progression in the Lewis Lung Carcinoma Orthotopic Mouse Model: A Comparison Between the Tail Vein Injection and Intranasal Instillation Methods.

Miki Yamada-Hara, Naoki Takahashi, Ji Won Byun, Liping Zeng, Zhihe Wang, Arisachi Tanaka, Zahra Malakoutikhah, Tomoko Hayashi, Nicholas J G Webster, Eyal Raz and 1 more

Abstract readComparative Study
In one paragraph

Article in Current protocols, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Miki Yamada-HaraDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Naoki TakahashiDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Ji Won ByunDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Liping ZengDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Zhihe WangDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Arisachi TanakaDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Zahra MalakoutikhahDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Tomoko HayashiMoores Cancer Center, University of California San Diego, La Jolla, California.
Nicholas J G WebsterDivision of Endocrinology, Department of Medicine, University of California San Diego, La Jolla, California.
Eyal RazDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.
Samuel BertinDivision of Rheumatology, Autoimmunity, and Inflammation, Department of Medicine, University of California San Diego, La Jolla, California.ORCID https://orcid.org/0000-0003-2340-959X

Funding

A novel pathway of Th17/Th2 induction: The role of cAMP signaling in DCR01HL141999 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RAZ, EYAL, WEBSTER, NICHOLAS J · 2019 to 2022
$2.9M
Chronic Exposure to House Dust Mites: A New Risk Factor for Lung Cancer in Never SmokersU01CA276642 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Samuel P Bertin, Eyal Raz · 2023 to 2026
$2.4M
SRSF3 degradation in liver disease and hepatocellular carcinomaI01BX004848 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI WEBSTER, NICHOLAS J · 2020 to 2025
–
BLR&D Research Career Scientist Award ApplicationIK6BX005224 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI WEBSTER, NICHOLAS J · 2020 to 2025
–
BLRD VA I01 BX004848BLRD VA IK6 BX005224NCI NIH HHS U01 CA276642NHLBI NIH HHS R01 HL141999
6 · The paper itself

Abstract

Metastasis remains a leading cause of cancer-related mortality, yet its study has been constrained by the lack of reliable animal models that faithfully replicate this complex process. Syngeneic models for studying lung cancer metastasis are limited, with the Lewis lung carcinoma (LLC) model being the most commonly employed. The conventional LLC orthotopic model involves injecting LLC cells intravenously (i.v.) via the tail vein into syngeneic C57BL/6 mice. However, this model has significant drawbacks, such as tumor development in multiple anatomical sites, incomplete lung tumor penetrance, and challenges in monitoring lung tumor growth. This article highlights the advantages of using luciferase-expressing LLC cells combined with bioluminescence imaging (BLI) to quantify tumor progression in live animals. We demonstrate that both white- and black-furred C57BL/6 mice can be used for BLI. Finally, we propose that intranasal (i.n.) instillation of LLC cells offers a valuable alternative to the traditional i.v. tail vein injection method, particularly for its simplicity and improved reproducibility. Although the LLC i.n. model does not recapitulate the metastasis process via the blood vascular route, it is an effective model for studying tumor seeding within the lungs and is particularly useful for analyzing the impact of the lung microenvironment on tumor initiation and progression. © 2024 Wiley Periodicals LLC. Basic Protocol 1: Lewis lung carcinoma intravenous injection method Support Protocol: In vivo bioluminescence imaging Basic Protocol 2: Lewis lung carcinoma intranasal instillation method.

Indexed as

Carcinoma, Lewis LungDisease Models, AnimalLuminescent MeasurementsMice, Inbred C57BLAdministration, IntranasalAnimalsCell Line, TumorDisease ProgressionInjections, IntravenousLuciferasesLung NeoplasmsMiceLuciferasesbioluminescence imagingin vivo modelsLewis lung carcinomalung cancermetastasis

Identifiers

PMID39660610
PMCPMC11649249

What OpenQuestion holds

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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.