New insights into RAS in head and neck cancer

被引:5
作者
Jagadeeshan, Sankar [1 ,2 ,9 ]
Novoplansky, Ofra Z. [1 ,2 ]
Cohen, Oded [2 ,3 ]
Kurth, Ina [4 ]
Hess, Jochen [5 ,6 ]
Rosenberg, Ari J. [7 ]
Grandis, Jennifer R. [8 ]
Elkabets, Moshe [1 ,2 ,9 ]
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Shraga Segal Dept Microbiol Immunol & Genet, POB 653, IL-8410501 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Fac Hlth Sci, POB 653, IL-8410501 Beer Sheva, Israel
[3] Soroka Med Ctr, Dept Otolaryngol Head & Neck Surg & Oncol, Beer Sheva, Israel
[4] German Canc Res Ctr, Div Radiobiol Radiooncol, Heidelberg, Germany
[5] Heidelberg Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, D-69120 Heidelberg, Germany
[6] German Canc Res Ctr, Mol Mech Head & Neck Tumors, D-69120 Heidelberg, Germany
[7] Univ Chicago, Dept Med, Sect Hematol & Oncol, Chicago, IL USA
[8] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, San Francisco, CA USA
[9] Ben Gurion Univ Negev, Fac Hlth Sci, Shraga Segal Dept Microbiol Immunol & Genet, IL-84105 Beer Sheva, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2023年 / 1878卷 / 06期
基金
以色列科学基金会;
关键词
Head and neck cancer; RAS activation; Therapy resistance; Progression; Metastasis; Pre-clinical and clinical targeting; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; LYMPH-NODE METASTASIS; H-RAS; ONCOGENIC-RAS; ORAL-CANCER; SIGNALING PATHWAYS; HUMAN-PAPILLOMAVIRUS; THERAPEUTIC TARGET; UP-REGULATION;
D O I
10.1016/j.bbcan.2023.188963
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RAS genes are known to be dysregulated in cancer for several decades, and substantial effort has been dedicated to develop agents that reduce RAS expression or block RAS activation. The recent introduction of RAS inhibitors for cancer patients highlights the importance of comprehending RAS alterations in head and neck cancer (HNC). In this regard, we examine the published findings on RAS alterations and pathway activations in HNC, and summarize their role in HNC initiation, progression, and metastasis. Specifically, we focus on the intrinsic role of mutated-RAS on tumor cell signaling and its extrinsic role in determining tumor-microenvironment (TME) heterogeneity, including promoting angiogenesis and enhancing immune escape. Lastly, we summarize the intrinsic and extrinsic role of RAS alterations on therapy resistance to outline the potential of targeting RAS using a single agent or in combination with other therapeutic agents for HNC patients with RAS-activated tumors.
引用
收藏
页数:24
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