FAM99B

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FAM99B may serve as a tumor suppressor in HCC and may provide a promising therapy target for patients with HCC.

Annotated Information

Name

Approved symbol:FAM99B

Approved name:family with sequence similarity 99 member B

HGNC ID:32369

Previous name:family with sequence similarity 99, member B|family with sequence similarity 99, member B (non-protein coding)|family with sequence similarity 99 member B (non-protein coding)

Alias symbol:DKFZp781M09150

RefSeq IDNR_:026642

LncBook ID:[1]

pubmed_id 31243545

Characteristics

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Function

FAM99B may serve as a tumor suppressor in HCC and may provide a promising therapy target for patients with HCC. [1].

EMS cooperates with the RNA binding protein RALY to stabilize E2F1 mRNA, and thereby increases E2F1 expression[1].

Regulation

Downregulated FAM99B was significantly associated with vascular invasion, advanced histologic grade, and T stage. [1].

Expression

Decreased FAM99B levels were significantly associated with poor overall survival in patients with HCC. Moreover, overexpression of FAM99B significantly inhibited cell proliferation, migration, and invasion in vitro. [1].

Diseases

  • Preeclampsia (PE)[1].

Labs working on this lncRNA

  • Department of Epidemiology, School of Public Health, Guangxi Medical University, Nanning, 530021, Guangxi, People's Republic of China.[1]
  • Department of Epidemiology and Statistics, School of Public Health, Guilin Medical University, Guilin, 541004, Guangxi, People's Republic of China.[1]
  • Department of Sanitary Chemistry, School of Public Health, Guangxi Medical University, Nanning, 530021, Guangxi, People's Republic of China.[1]
  • Department of Epidemiology, School of Public Health, Guangxi Medical University, Nanning, 530021, Guangxi, People's Republic of China. xqqiu9999@sina.com.[1]

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 Mo M, Liu S, Ma X, Tan C, Wei L, Sheng Y, Song Y, Zeng X, Huang D, Qiu X. A liver-specific lncRNA, FAM99B, suppresses hepatocellular carcinoma progression through inhibition of cell proliferation, migration, and invasion. J Cancer Res Clin Oncol. 2019 Aug;145(8):2027-2038. doi: 10.1007/s00432-019-02954-8. Epub 2019 Jun 26. PMID: 31243545.