Fibroblast growth factor 8(FGF-8) is a protein that in humans is encoded by the FGF8gene.[5][6][7]
Function
The protein encoded by this gene belongs to the fibroblast growth factor (FGF) family. FGF proteins are multifunctional signaling molecules with broad mitogenic and cell survival activity, playing critical roles in embryonic development, cell proliferation, morphogenesis, tissue repair, and tumor progression.[8] FGF8 signals primarily through fibroblast growth factor receptor 1 (FGFR1) to trigger downstream pathways involved in neural and limb development.[9]
Neural development and brain patterning
FGF8 is essential for establishing the midbrain–hindbrain boundary (mesencephalon/metencephalon), a key signaling center during brain development. This region is defined by cross-repression between Otx2 and Gbx2, which helps maintain FGF8 expression. FGF8 then induces the expression of transcription factors, forming feedback loops that guide the development of the midbrain and hindbrain.[10][11]
In the forebrain, FGF8 helps define cortical areas by regulating transcription factors such as Emx2, Pax6, COUP-TF1, and COUP-TF2. These factors are expressed in opposing gradients and interact to establish the anterior–posterior patterning of the cerebral cortex.[12][13]
Patterning of body axes and germ layers
FGF8 plays a pivotal role in early embryonic patterning, influencing the development of all three germ layers. In the mesoderm, FGF8 helps regulate somite formation through the Clock and wavefront model, promoting segmentation and the establishment of anterior–posterior identity.[14][15]
In the endoderm, FGF8 acts in coordination with retinoic acid (RA) to direct organ specification. Low levels of FGF8 promote the formation of anterior endodermal derivatives such as the liver and pancreas,[16] while higher levels specify posterior structures such as the hindgut.[17]
Limb development and morphogenesis
FGF8 is secreted by the apical ectodermal ridge (AER) at the distal end of limb buds and is essential for limb initiation, patterning, and outgrowth.[18] Loss of FGF8 results in limb reduction or absence, with forelimbs and proximal segments being most affected.[19] FGF8 also influences Sonic hedgehog (Shh) signaling and is involved in tendon and digit formation.[20][21]
Craniofacial development
FGF8 also contributes to craniofacial development, including the formation of the teeth, palate, mandible, and salivary glands. Altered expression can result in craniofacial abnormalities such as cleft palate, mandibular hypoplasia, or tooth agenesis.[22] In conclusion, FGF8 expression has effects on a person’s facial appearance, brain, lungs,
heart, kidneys, and limbs. If there is not enough FGF8 or too much, there can be defects in all of
these systems like limb loss, cleft lip/ palate, kidney disease, and neurodevelopmental defects.
Clinical significance
This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogenesis. The adult expression of this gene was once thought to be restricted to testes and ovaries but has been described in several organ systems.[23] Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs reveal roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants.[24]
FGF8 has been documented to play a role in oralmaxillogacial diseases and CRISPR-cas9 gene targeting on FGF8 may be key in treating these diseases. Cleft lip and/or palate (CLP) genome wide gene analysis shows a D73H missense mutation in the FGF8 gene[22] which reduces the binding affinity of FGF8. Loss of TBX1 and Tfap2 can result in proliferation and apoptosis in the palate cells increasing the risk of CLP. Overexpression of FGF8 due to misregulation of the Gli processing gene may result in cliliopathies. Agnathia, a malformation of the mandible, is often a lethal condition that comes from the absence of BMP4 regulators (noggin and chordin), resulting in high levels of BMP4 signaling, which in turn drastically reduces FGF8 signaling, increasing cell death during mandibular outgrowth.[22] Lastly, the ability for FGF8 to regulate cell proliferation has caused interest in its effects on tumors or squamous cell carcinoma. CRISPR-cas9 gene targeting methods are currently being studied to determine if they are the key to solving FGF8 mutations associated with oral diseases.
Knockout models
FGF-8 knockout models have led to lethality in gastrulating state embryos in mice models.[25] Research has demonstrated that decreased expression of FGF-8 can alter the cleft lip pathology in mice.[26] However, due to the importance that FGF-8 has in the development and programming in multiple organ systems, full "knockout" models have led to embryonic death in multiple studies, limiting the ability to study the removal of the morphogen in adult models.[27] While knockout experiments have occurred with this gene, a lack of/mutation in FGF8 in the early stages of embryo development is lethal. Disruption of the gene in later developmental stages has caused several issues with limb formation and development. Researchers hope to determine a way to study the signaling molecule in the future to investigate how to prevent defects including Kallmann syndrome.
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Yoshiura K, Leysens NJ, Chang J, Ward D, Murray JC, Muenke M (October 1997). "Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes". American Journal of Medical Genetics. 72 (3): 354–362. doi:10.1002/(SICI)1096-8628(19971031)72:3<354::AID-AJMG21>3.0.CO;2-R. PMID9332670.
^Gemel J, Gorry M, Ehrlich GD, MacArthur CA (July 1996). "Structure and sequence of human FGF8". Genomics. 35 (1): 253–257. doi:10.1006/geno.1996.0349. PMID8661131.
^White RA, Dowler LL, Angeloni SV, Pasztor LM, MacArthur CA (November 1995). "Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region". Genomics. 30 (1): 109–111. doi:10.1006/geno.1995.0020. PMID8595889.
^Harris WA, Sanes DH, Reh TA (2011). Development of the Nervous System, Third Edition. Boston: Academic Press. pp. 33–34. ISBN978-0-12-374539-2.
^Crossley PH, Martin GR (February 1995). "The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo". Development. 121 (2): 439–451. doi:10.1242/dev.121.2.439. PMID7768185.
^Lewandoski M, Sun X, Martin GR (December 2000). "Fgf8 signalling from the AER is essential for normal limb development". Nature Genetics. 26 (4): 460–463. doi:10.1038/82609. PMID11101846. S2CID28105181.
^Hao Y, Tang S, Yuan Y, Liu R, Chen Q (March 2019). "Roles of FGF8 subfamily in embryogenesis and oral‑maxillofacial diseases (Review)". International Journal of Oncology. 54 (3): 797–806. doi:10.3892/ijo.2019.4677. PMID30628659.
Gemel J, Gorry M, Ehrlich GD, MacArthur CA (July 1996). "Structure and sequence of human FGF8". Genomics. 35 (1): 253–257. doi:10.1006/geno.1996.0349. PMID8661131.
Payson RA, Wu J, Liu Y, Chiu IM (July 1996). "The human FGF-8 gene localizes on chromosome 10q24 and is subjected to induction by androgen in breast cancer cells". Oncogene. 13 (1): 47–53. PMID8700553.
Ghosh AK, Shankar DB, Shackleford GM, Wu K, T'Ang A, Miller GJ, et al. (October 1996). "Molecular cloning and characterization of human FGF8 alternative messenger RNA forms". Cell Growth & Differentiation. 7 (10): 1425–1434. PMID8891346.
Yoshiura K, Leysens NJ, Chang J, Ward D, Murray JC, Muenke M (October 1997). "Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes". American Journal of Medical Genetics. 72 (3): 354–362. doi:10.1002/(SICI)1096-8628(19971031)72:3<354::AID-AJMG21>3.0.CO;2-R. PMID9332670.
Loo BB, Darwish KK, Vainikka SS, Saarikettu JJ, Vihko PP, Hermonen JJ, et al. (May 2000). "Production and characterization of the extracellular domain of recombinant human fibroblast growth factor receptor 4". The International Journal of Biochemistry & Cell Biology. 32 (5): 489–497. doi:10.1016/S1357-2725(99)00145-4. PMID10736564.
Xu J, Liu Z, Ornitz DM (May 2000). "Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures". Development. 127 (9): 1833–1843. doi:10.1242/dev.127.9.1833. PMID10751172.
Tanaka S, Ueo H, Mafune K, Mori M, Wands JR, Sugimachi K (May 2001). "A novel isoform of human fibroblast growth factor 8 is induced by androgens and associated with progression of esophageal carcinoma". Digestive Diseases and Sciences. 46 (5): 1016–1021. doi:10.1023/A:1010753826788. PMID11341643. S2CID30175286.
Ruohola JK, Viitanen TP, Valve EM, Seppänen JA, Loponen NT, Keskitalo JJ, et al. (May 2001). "Enhanced invasion and tumor growth of fibroblast growth factor 8b-overexpressing MCF-7 human breast cancer cells". Cancer Research. 61 (10): 4229–4237. PMID11358849.
Mattila MM, Ruohola JK, Valve EM, Tasanen MJ, Seppänen JA, Härkönen PL (May 2001). "FGF-8b increases angiogenic capacity and tumor growth of androgen-regulated S115 breast cancer cells". Oncogene. 20 (22): 2791–2804. doi:10.1038/sj.onc.1204430. PMID11420691. S2CID22624526.