The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer

The finely tuned integration of intra- and extracellular cues by components of the mitogen-activated protein kinase (MAPK) signaling pathways controls the mutually exclusive phenotypic manifestations of uncontrolled growth and tumor cell dissemination. The Ser/Thr kinase MAP4K4 is an upstream integr...

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Main Authors: Dejana Jovanovic, Shen Yan, Martin Baumgartner
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.1059513/full
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author Dejana Jovanovic
Shen Yan
Martin Baumgartner
author_facet Dejana Jovanovic
Shen Yan
Martin Baumgartner
author_sort Dejana Jovanovic
collection DOAJ
description The finely tuned integration of intra- and extracellular cues by components of the mitogen-activated protein kinase (MAPK) signaling pathways controls the mutually exclusive phenotypic manifestations of uncontrolled growth and tumor cell dissemination. The Ser/Thr kinase MAP4K4 is an upstream integrator of extracellular cues involved in both proliferation and cell motility control. Initially identified as an activator of the c-Jun N-terminal kinase (JNK), the discovery of diverse functions and additional effectors of MAP4K4 beyond JNK signaling has considerably broadened our understanding of this complex kinase. The implication of MAP4K4 in the regulation of cytoskeleton dynamics and cell motility provided essential insights into its role as a pro-metastatic kinase in cancer. However, the more recently revealed role of MAP4K4 as an activator of the Hippo tumor suppressor pathway has complicated the understanding of MAP4K4 as an oncogenic driver kinase. To develop a better understanding of the diverse functions of MAP4K4 and their potential significance in oncogenesis and tumor progression, we have collected and assessed the current evidence of MAP4K4 implication in molecular mechanisms that control proliferation and promote cell motility. A better understanding of these mechanisms is particularly relevant in the brain, where MAP4K4 is highly expressed and under pathological conditions either drives neuronal cell death in neurodegenerative diseases or cell dissemination in malignant tumors. We review established effectors and present novel interactors of MAP4K4, which offer mechanistic insights into MAP4K4 function and may inspire novel intervention strategies. We discuss possible implications of novel interactors in tumor growth and dissemination and evaluate potential therapeutic strategies to selectively repress pro-oncogenic functions of MAP4K4.
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spelling doaj.art-6caf5fb8ff754f6985115f4fe4587b282022-12-22T02:57:15ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-12-011210.3389/fonc.2022.10595131059513The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancerDejana JovanovicShen YanMartin BaumgartnerThe finely tuned integration of intra- and extracellular cues by components of the mitogen-activated protein kinase (MAPK) signaling pathways controls the mutually exclusive phenotypic manifestations of uncontrolled growth and tumor cell dissemination. The Ser/Thr kinase MAP4K4 is an upstream integrator of extracellular cues involved in both proliferation and cell motility control. Initially identified as an activator of the c-Jun N-terminal kinase (JNK), the discovery of diverse functions and additional effectors of MAP4K4 beyond JNK signaling has considerably broadened our understanding of this complex kinase. The implication of MAP4K4 in the regulation of cytoskeleton dynamics and cell motility provided essential insights into its role as a pro-metastatic kinase in cancer. However, the more recently revealed role of MAP4K4 as an activator of the Hippo tumor suppressor pathway has complicated the understanding of MAP4K4 as an oncogenic driver kinase. To develop a better understanding of the diverse functions of MAP4K4 and their potential significance in oncogenesis and tumor progression, we have collected and assessed the current evidence of MAP4K4 implication in molecular mechanisms that control proliferation and promote cell motility. A better understanding of these mechanisms is particularly relevant in the brain, where MAP4K4 is highly expressed and under pathological conditions either drives neuronal cell death in neurodegenerative diseases or cell dissemination in malignant tumors. We review established effectors and present novel interactors of MAP4K4, which offer mechanistic insights into MAP4K4 function and may inspire novel intervention strategies. We discuss possible implications of novel interactors in tumor growth and dissemination and evaluate potential therapeutic strategies to selectively repress pro-oncogenic functions of MAP4K4.https://www.frontiersin.org/articles/10.3389/fonc.2022.1059513/fullMAP4K4proliferationmotilitySTRIPAK complexactin dynamicsPKC delta
spellingShingle Dejana Jovanovic
Shen Yan
Martin Baumgartner
The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
Frontiers in Oncology
MAP4K4
proliferation
motility
STRIPAK complex
actin dynamics
PKC delta
title The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
title_full The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
title_fullStr The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
title_full_unstemmed The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
title_short The molecular basis of the dichotomous functionality of MAP4K4 in proliferation and cell motility control in cancer
title_sort molecular basis of the dichotomous functionality of map4k4 in proliferation and cell motility control in cancer
topic MAP4K4
proliferation
motility
STRIPAK complex
actin dynamics
PKC delta
url https://www.frontiersin.org/articles/10.3389/fonc.2022.1059513/full
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