Myotubularin-related protein 7 inhibits insulin signaling in colorectal cancer

被引:24
|
作者
Weidner, Philip [1 ]
Soehn, Michaela [1 ]
Gutting, Tobias [1 ]
Friedrich, Teresa [1 ]
Gaiser, Timo [2 ]
Magdeburg, Julia [3 ]
Kienle, Peter [3 ]
Ruh, Hermelindis [4 ]
Hopf, Carsten [4 ]
Behrens, Hans-Michael [5 ]
Roecken, Christoph [5 ]
Hanoch, Tamar [6 ]
Seger, Rony [6 ]
Ebert, Matthias P. A. [1 ]
Burgermeister, Elke [1 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Univ Med Mannheim, Dept Med 2, D-68167 Mannheim, Germany
[2] Heidelberg Univ, Med Fac Mannheim, Univ Med Mannheim, Inst Pathol, D-68167 Mannheim, Germany
[3] Heidelberg Univ, Med Fac Mannheim, Univ Med Mannheim, Dept Surg, D-68167 Mannheim, Germany
[4] Mannheim Univ Appl Sci, ABIMAS Res Ctr, D-68163 Mannheim, Germany
[5] Univ Kiel, Inst Pathol, D-24105 Kiel, Germany
[6] Weizmann Inst Sci, Dept Biol Regulat, I-7610001 Rehovot, Israel
关键词
colorectal cancer; insulin; MTMR7; phosphatase; myotubularin; GASTRIC-CANCER; METAANALYSIS; PROGRESSION; RECURRENCE; CAVEOLIN-1; EXPRESSION; MUTATIONS; AUTOPHAGY; GENOMICS; FAMILY;
D O I
10.18632/oncotarget.10466
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phosphoinositide (PIP) phosphatases such as myotubularins (MTMs) inhibit growth factor receptor signaling. However, the function of myotubularin-related protein 7 (MTMR7) in cancer is unknown. We show that MTMR7 protein was down-regulated with increasing tumor grade (G), size (T) and stage (UICC) in patients with colorectal cancer (CRC) (n=1786). The presence of MTMR7 in the stroma correlated with poor prognosis, whereas MTMR7 expression in the tumor was not predictive for patients' survival. Insulin reduced MTMR7 protein levels in human CRC cell lines, and CRC patients with type 2 diabetes mellitus (T2DM) or loss of imprinting (LOI) of insulin-like growth factor 2 (IGF2) had an increased risk for MTMR7 loss. Mechanistically, MTMR7 lowered PIPs and inhibited insulin-mediated AKT-ERK1/2 signaling and proliferation in human CRC cell lines. MTMR7 provides a novel link between growth factor signaling and cancer, and may thus constitute a potential marker or drug target for human CRC.
引用
收藏
页码:50490 / 50506
页数:17
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