Development of a novel murine model of lymphatic metastasis.


Journal

Clinical & experimental metastasis
ISSN: 1573-7276
Titre abrégé: Clin Exp Metastasis
Pays: Netherlands
ID NLM: 8409970

Informations de publication

Date de publication:
04 2020
Historique:
received: 09 08 2019
accepted: 27 01 2020
pubmed: 14 2 2020
medline: 17 9 2020
entrez: 14 2 2020
Statut: ppublish

Résumé

Current laboratory models of lymphatic metastasis generally require either genetically modified animals or are technically challenging. Herein, we have developed a robust protocol for the induction of intralymphatic metastasis in wild-type mice with reproducible outcomes. To determine an optimal injection quantity and timeline for tumorigenesis, C57Bl/6 mice were injected directly into the mesenteric lymph duct (MLD) with varying numbers of syngeneic murine colon cancer cells (MC38) or gastric cancer cells (YTN16) expressing GFP/luciferase and monitored over 2-4 weeks. Tumor growth was tracked via whole-animal in vivo bioluminescence imaging (IVIS). Our data indicate that the injection of tumor cells into the MLD is a viable model for lymphatic metastasis as necropsies revealed large tumor burdens and metastasis in regional lymph nodes. This protocol enables a closer study of the role of lymphatics in cancer metastasis and opens a window for the development of novel approaches for treatment of metastatic diseases.

Identifiants

pubmed: 32052231
doi: 10.1007/s10585-020-10025-3
pii: 10.1007/s10585-020-10025-3
pmc: PMC7979265
mid: NIHMS1680045
doi:

Substances chimiques

Green Fluorescent Proteins 147336-22-9
Luciferases EC 1.13.12.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

247-255

Subventions

Organisme : NIH HHS
ID : S10 OD021804
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA106183
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK058404
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA068485
Pays : United States
Organisme : NIDDK NIH HHS
ID : U25 DK059632
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK059637
Pays : United States

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Auteurs

Babak Banan (B)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

Jacob A Beckstead (JA)

Program in Cancer Biology, Department of Pharmacology, Vanderbilt University, Nashville, TN, USA.

Lauren E Dunavant (LE)

Program in Cancer Biology, Department of Pharmacology, Vanderbilt University, Nashville, TN, USA.

Yoojin Sohn (Y)

Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.

Jamie M Adcock (JM)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

Sachiyo Nomura (S)

Department of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Naji Abumrad (N)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

James R Goldenring (JR)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Nashville Veterans Affairs Medical Center, Nashville, TN, USA.

Barbara Fingleton (B)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA. barbara.fingleton@vanderbilt.edu.
Program in Cancer Biology, Department of Pharmacology, Vanderbilt University, Nashville, TN, USA. barbara.fingleton@vanderbilt.edu.

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