» Articles » PMID: 16132578

Syngeneic Mouse Mammary Carcinoma Cell Lines: Two Closely Related Cell Lines with Divergent Metastatic Behavior

Overview
Specialty Oncology
Date 2005 Sep 1
PMID 16132578
Citations 143
Authors
Affiliations
Soon will be listed here.
Abstract

Two cell lines, Met-1(fvb2) and DB-7(fvb2), with different metastatic potential, were derived from mammary carcinomas in FVB/N-Tg(MMTV-PyVmT) and FVB/N-Tg(MMTV-PyVmT ( Y315F/Y322F )) mice, transplanted into syngeneic FVB/N hosts and characterized. The lines maintain a stable morphological and biological phenotype after multiple rounds of in vitro culture and in vivo transplantation. The Met-1(fvb2) line derived from a FVB/N-Tg(MMTV-PyVmT) tumor exhibits invasive growth and 100% metastases when transplanted into the females FVB/N mammary fat pad. The DB-7(fvb2) line derived from the FVB/N-Tg(MMTV-PyVmT ( Y315F/Y322F )) with a "double base" modification at Y315F/Y322F exhibits more rapid growth when transplanted into the mammary fat pad, but a lower rate of metastasis (17%). The Met1(fvb2) cells show high activation of AKT, while DB-7(fvb2) cells show very low levels of AKT activation. The DNA content and gene expression levels of both cell lines are stable over multiple generations. Therefore, these two cell lines provide a stable, reproducible resource for the study of metastasis modulators, AKT molecular pathway interactions, and gene target and marker discovery.

Citing Articles

Neutrophils physically interact with tumor cells to form a signaling niche promoting breast cancer aggressiveness.

Camargo S, Moskowitz O, Giladi A, Levinson M, Balaban R, Gola S Nat Cancer. 2025; .

PMID: 40055573 DOI: 10.1038/s43018-025-00924-3.


The combined treatment with ketogenic diet and metformin slows tumor growth in two mouse models of triple negative breast cancer.

Schmidt K, Thatcher A, Grobe A, Broussard P, Hicks L, Gu H Transl Med Commun. 2024; 9(1).

PMID: 39574543 PMC: 11580796. DOI: 10.1186/s41231-024-00178-8.


Mcam stabilizes a luminal progenitor-like breast cancer cell state via Ck2 control and Src/Akt/Stat3 attenuation.

Balcioglu O, Gates B, Freeman D, Hagos B, Mehrabad E, Ayala-Talavera D NPJ Breast Cancer. 2024; 10(1):80.

PMID: 39277578 PMC: 11401886. DOI: 10.1038/s41523-024-00687-7.


A novel lipophilic amiloride derivative efficiently kills chemoresistant breast cancer cells.

Hu M, Liu R, Castro N, Loza Sanchez L, Rueankham L, Learn J Sci Rep. 2024; 14(1):20263.

PMID: 39217266 PMC: 11365969. DOI: 10.1038/s41598-024-71181-0.


Natural Killer Cell Regulation of Breast Cancer Stem Cells Mediates Metastatic Dormancy.

Bushnell G, Sharma D, Wilmot H, Zheng M, Fashina T, Hutchens C Cancer Res. 2024; 84(20):3337-3353.

PMID: 39106452 PMC: 11474167. DOI: 10.1158/0008-5472.CAN-24-0030.


References
1.
Basu G, Pathangey L, Tinder T, Lagioia M, Gendler S, Mukherjee P . Cyclooxygenase-2 inhibitor induces apoptosis in breast cancer cells in an in vivo model of spontaneous metastatic breast cancer. Mol Cancer Res. 2004; 2(11):632-42. View

2.
Webster M, Hutchinson J, Rauh M, Muthuswamy S, Anton M, Tortorice C . Requirement for both Shc and phosphatidylinositol 3' kinase signaling pathways in polyomavirus middle T-mediated mammary tumorigenesis. Mol Cell Biol. 1998; 18(4):2344-59. PMC: 121489. DOI: 10.1128/MCB.18.4.2344. View

3.
Cozma D, Lukes L, Rouse J, Qiu T, Liu E, Hunter K . A bioinformatics-based strategy identifies c-Myc and Cdc25A as candidates for the Apmt mammary tumor latency modifiers. Genome Res. 2002; 12(6):969-75. PMC: 1383737. DOI: 10.1101/gr.210502. View

4.
Bourguignon L, Iida N, Zhu H, Young L, Muller W, Cardiff R . CD44v(3,8-10) is involved in cytoskeleton-mediated tumor cell migration and matrix metalloproteinase (MMP-9) association in metastatic breast cancer cells. J Cell Physiol. 1998; 176(1):206-15. DOI: 10.1002/(SICI)1097-4652(199807)176:1<206::AID-JCP22>3.0.CO;2-3. View

5.
Jemal A, Tiwari R, Murray T, Ghafoor A, Samuels A, Ward E . Cancer statistics, 2004. CA Cancer J Clin. 2004; 54(1):8-29. DOI: 10.3322/canjclin.54.1.8. View