Roles of Aldolase Family Genes in Human Cancers and Diseases

被引:117
作者
Chang, Yu-Chan [1 ]
Yang, Yi-Chieh [1 ,2 ]
Tien, Chia-Ping [3 ]
Yang, Chih-Jen [4 ,5 ,6 ]
Hsiao, Michael [1 ,7 ]
机构
[1] Acad Sinica, Genom Res Ctr, Taipei, Taiwan
[2] Taipei Med Univ, Grad Inst Clin Med, Coll Med, Taipei, Taiwan
[3] China Med Univ Hosp, Dept Family Med, Taichung, Taiwan
[4] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Div Pulm & Crit Care Med, Dept Internal Med, Kaohsiung, Taiwan
[5] Kaohsiung Med Univ, Sch Med, Coll Med, Kaohsiung, Taiwan
[6] Kaohsiung Med Univ, Kaohsiung Municipal Ta Tung Hosp, Dept Internal Med, Kaohsiung, Taiwan
[7] Kaohsiung Med Univ, Coll Med, Dept Biochem, Kaohsiung, Taiwan
关键词
GLYCOLYTIC-ENZYMES; POOR-PROGNOSIS; TUMOR MICROENVIRONMENT; CELL-PROLIFERATION; DIRECTLY INTERACTS; PANCREATIC-CANCER; EXPRESSION; METABOLISM; ALDOB; PATHWAY;
D O I
10.1016/j.tem.2018.05.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aldolase family members involved in metabolism and glycolysis are present in three isoforms: ALDOA, ALDOB, and ALDOC. Aldolases are differentially expressed in human tissues, and aberrant expression has been observed in several human diseases and cancer types. However, non-enzymatic functions through protein-protein interactions or epigenetic modifications have been reported in recent years. Using high-throughput screening and -omics database integration, aldolase has been validated as an independent clinical prognostic marker of human cancers. Therefore, the aim of this review was to provide potential clinical value from in silico predictions and also summarize well-known signaling axes or phenotypes in various cancer types. Finally, we discuss the role of aldolase in the treatment of human diseases and cancers.
引用
收藏
页码:549 / 559
页数:11
相关论文
共 85 条
  • [1] Hereditary fructose intolerance
    Ali, M
    Rellos, P
    Cox, TM
    [J]. JOURNAL OF MEDICAL GENETICS, 1998, 35 (05) : 353 - 365
  • [2] MCT4 Defines a Glycolytic Subtype of Pancreatic Cancer with Poor Prognosis and Unique Metabolic Dependencies
    Baek, GuemHee
    Tse, Yan F.
    Hu, Zeping
    Cox, Derek
    Buboltz, Noah
    McCue, Peter
    Yeo, Charles J.
    White, Michael A.
    DeBerardinis, Ralph J.
    Knudsen, Erik S.
    Witkiewicz, Agnieszka K.
    [J]. CELL REPORTS, 2014, 9 (06): : 2233 - 2249
  • [3] Bijarnia-Mahay S, 2015, JIMD REP, V19, P85, DOI 10.1007/8904_2014_374
  • [4] Aldolase positively regulates of the canonical Wnt signaling pathway
    Caspi, Michal
    Perry, Gili
    Skalka, Nir
    Meisel, Shilhav
    Firsow, Anastasia
    Amit, Maayan
    Rosin-Arbesfeld, Rina
    [J]. MOLECULAR CANCER, 2014, 13
  • [5] Metabolic control of primed human pluripotent stem cell fate and function by the miR-200c-SIRT2 axis
    Cha, Young
    Han, Min-Joon
    Cha, Hyuk-Jin
    Zoldan, Janet
    Burkart, Alison
    Jung, Jin Hyuk
    Jang, Yongwoo
    Kim, Chun-Hyung
    Jeong, Ho-Chang
    Kim, Byung-Gyu
    Langer, Robert
    Kahn, C. Ronald
    Guarente, Leonard
    Kim, Kwang-Soo
    [J]. NATURE CELL BIOLOGY, 2017, 19 (05) : 445 - +
  • [6] Metabolic Competition in the Tumor Microenvironment Is a Driver of Cancer Progression
    Chang, Chih-Hao
    Qiu, Jing
    O'Sullivan, David
    Buck, Michael D.
    Noguchi, Takuro
    Curtis, Jonathan D.
    Chen, Qiongyu
    Gindin, Mariel
    Gubin, Matthew M.
    van der Windt, Gerritje J. W.
    Tonc, Elena
    Schreiber, Robert D.
    Pearce, Edward J.
    Pearce, Erika L.
    [J]. CELL, 2015, 162 (06) : 1229 - 1241
  • [7] Feedback regulation of ALDOA activates the HIF-1 α/MMP9 axis to promote lung cancer progression
    Chang, Yu-Chan
    Chan, Yung-Chieh
    Chang, Wei-Ming
    Lin, Yuan-Feng
    Yang, Chih-Jen
    Su, Chia-Yi
    Huang, Ming-Shyan
    Wu, Alexander T. H.
    Hsiao, Michael
    [J]. CANCER LETTERS, 2017, 403 : 28 - 36
  • [8] Chang YC, 2017, J HEMATOL ONCOL, V10, DOI [10.1186/s13045-016-0372-0, 10.22834/PDS.2017.10.3.1]
  • [9] Proteomic Profiling of Osteosarcoma Cells Identifies ALDOA and SULT1A3 as Negative Survival Markers of Human Osteosarcoma
    Chen, Xiang
    Yang, Tong-Tao
    Zhou, Yong
    Wang, Wei
    Qiu, Xiu-Chun
    Gao, Jie
    Li, Cun-Xiao
    Long, Hua
    Ma, Bao-An
    Ma, Qiong
    Zhang, Xian-zhi
    Yang, Lian-Jia
    Fan, Qing-Yu
    [J]. MOLECULAR CARCINOGENESIS, 2014, 53 (02) : 138 - 144
  • [10] A Novel Frameshift Mutation of the ALDOB Gene in a Korean Girl Presenting with Recurrent Hepatitis Diagnosed as Hereditary Fructose Intolerance
    Choi, Hae-Won
    Lee, Yeoun Joo
    Oh, Seak Hee
    Kim, Kyung Mo
    Ryu, Jeong-Min
    Lee, Beom Hee
    Kim, Gu-Hwan
    Yoo, Han-Wook
    [J]. GUT AND LIVER, 2012, 6 (01) : 126 - 128