Forced over-expression of the myeloid zinc finger gene MZF-1 inhibits apoptosis and promotes oncogenesis in interleukin-3-dependent FDCP.1 cells

R. Hromas; S. Boswell; R. N. Shen; G. Burgess; A. Davidson; K. Cornetta; J. Sutton; K. Robertson

Forced over-expression of the myeloid zinc finger gene MZF-1 inhibits apoptosis and promotes oncogenesis in interleukin-3-dependent FDCP.1 cells

R. Hromas
, S. Boswell
, R. N. Shen
, G. Burgess
, A. Davidson
, K. Cornetta
, J. Sutton
, K. Robertson

Research output: Contribution to journal › Article › peer-review

Abstract

The myeloid zinc finger protein MZF-1 is important in hematopoiesis. Previous studies have found that reducing expression of MZF-1 inhibited G-CSF-driven human marrow colony formation assays. In this study we found that retrovirally overexpressing MZF-1 in IL-3 dependent FDCP.1 cells inhibited their apoptosis when IL-3 was withdrawn. The MZF-1-transduced FDCP.1 cells also formed tumors when injected into congenic mice, whereas control FDCP.1 cells did not.

Original language	English (US)
Pages (from-to)	1049-1050
Number of pages	2
Journal	Leukemia
Volume	10
Issue number	6
State	Published - Jun 1996
Externally published	Yes

Keywords

Apoptosis
Oncogenesis
Retroviral gene transfer
Transcription factors

ASJC Scopus subject areas

Hematology
Oncology
Cancer Research

Cite this

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title = "Forced over-expression of the myeloid zinc finger gene MZF-1 inhibits apoptosis and promotes oncogenesis in interleukin-3-dependent FDCP.1 cells",

abstract = "The myeloid zinc finger protein MZF-1 is important in hematopoiesis. Previous studies have found that reducing expression of MZF-1 inhibited G-CSF-driven human marrow colony formation assays. In this study we found that retrovirally overexpressing MZF-1 in IL-3 dependent FDCP.1 cells inhibited their apoptosis when IL-3 was withdrawn. The MZF-1-transduced FDCP.1 cells also formed tumors when injected into congenic mice, whereas control FDCP.1 cells did not.",

keywords = "Apoptosis, Oncogenesis, Retroviral gene transfer, Transcription factors",

author = "R. Hromas and S. Boswell and Shen, \{R. N.\} and G. Burgess and A. Davidson and K. Cornetta and J. Sutton and K. Robertson",

year = "1996",

month = jun,

language = "English (US)",

volume = "10",

pages = "1049--1050",

journal = "Leukemia",

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TY - JOUR

T1 - Forced over-expression of the myeloid zinc finger gene MZF-1 inhibits apoptosis and promotes oncogenesis in interleukin-3-dependent FDCP.1 cells

AU - Hromas, R.

AU - Boswell, S.

AU - Shen, R. N.

AU - Burgess, G.

AU - Davidson, A.

AU - Cornetta, K.

AU - Sutton, J.

AU - Robertson, K.

PY - 1996/6

Y1 - 1996/6

N2 - The myeloid zinc finger protein MZF-1 is important in hematopoiesis. Previous studies have found that reducing expression of MZF-1 inhibited G-CSF-driven human marrow colony formation assays. In this study we found that retrovirally overexpressing MZF-1 in IL-3 dependent FDCP.1 cells inhibited their apoptosis when IL-3 was withdrawn. The MZF-1-transduced FDCP.1 cells also formed tumors when injected into congenic mice, whereas control FDCP.1 cells did not.

AB - The myeloid zinc finger protein MZF-1 is important in hematopoiesis. Previous studies have found that reducing expression of MZF-1 inhibited G-CSF-driven human marrow colony formation assays. In this study we found that retrovirally overexpressing MZF-1 in IL-3 dependent FDCP.1 cells inhibited their apoptosis when IL-3 was withdrawn. The MZF-1-transduced FDCP.1 cells also formed tumors when injected into congenic mice, whereas control FDCP.1 cells did not.

KW - Apoptosis

KW - Oncogenesis

KW - Retroviral gene transfer

KW - Transcription factors

UR - https://www.scopus.com/pages/publications/0030018316

UR - https://www.scopus.com/pages/publications/0030018316#tab=citedBy

M3 - Article

C2 - 8667641

AN - SCOPUS:0030018316

SN - 0887-6924

VL - 10

SP - 1049

EP - 1050

JO - Leukemia

JF - Leukemia

IS - 6

ER -

Forced over-expression of the myeloid zinc finger gene MZF-1 inhibits apoptosis and promotes oncogenesis in interleukin-3-dependent FDCP.1 cells

Abstract

Keywords

ASJC Scopus subject areas

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