Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia

• Published in: Molecular biology reports Vol. 50; no. 1; pp. 931 - 936
• Main Authors: Behera, Chinmay Kumar, Gyandeep, Gummalla, Mishra, Reshmi, Mohanty, Rashmi Priya, Pal, Aditi, Behera, Jyotika, Samal, Sagnika, Das, Biswadeep
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 2023; Springer Nature B.V
• Subjects: Acute myeloid leukemia; Amino acids; Anemia; Animal Anatomy; Animal Biochemistry; Aplastic anemia; Biomedical and Life Sciences; Biopsy; Blast cells; Bone marrow; Cell culture; Chromosome 3; Cytogenetics; Dengue fever; Dengue hemorrhagic fever; DNA-Binding Proteins - genetics; Exons; FANCC protein; Fanconi Anemia - genetics; Fanconi Anemia Complementation Group F Protein - genetics; Fanconi syndrome; Female; Genetic disorders; Genomes; Hereditary diseases; Histology; Humans; Immunoglobulin M; Leukemia; Leukemia, Myeloid, Acute - genetics; Life Sciences; Lymphocytes; Minority & ethnic groups; Morphology; Mutation; Mutation - genetics; Pathogenicity; Patients; Pediatrics; Phenotypes; Short Communication; Stop codon; India; Thumb aplasia; Chromosomal breakage analysis; Fanconi anemia; Whole genome sequencing; FANCF gene
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-022-08071-z

Background Fanconi anemia (FA) is a rare genetic disorder and one of the most common inherited forms of aplastic anemia. FA is an autosomal recessive or X-linked genetic disorder that is characterized by typical physical malformations and haematopoietic anomalies. In most cases of FA, patients harbor homozygous or double heterozygous mutations in the FANCA (60–65%), FANCC (10–15%), FANCG (~ 10%), FANCD2 (3–6%) or FANCF (2%) genes in different ethnic populations, which leads to inherited bone marrow failure (IBMF). Hence, it is important to screen such mutations in correlation with clinical manifestations of FA in various ethnic populations. Approach An 11 year old female pediatric patient of an East India family was presented with febrile illness, having thrombocytopenia with positive dengue IgM (Immunoglobulin M) and treated as a case of dengue hemorrhagic fever at the initial stage of diagnosis. Chromosomal breakage study was performed based on the abnormal physical examination, which showed 100% breaks, triradials, and quadrilaterals in mitomycin (MMC)-induced peripheral blood lymphocyte culture. Importantly, conventional cytogenetic assay in most of the bone marrow cells revealed an additional gain in chromosome 3q+ [46,XX,add(3)(q25)] and terminal loss in chr8p- [46,XX,del(8)(p23)], which might have a prognostic relevance in the outcomes of the FA patient. The bone marrow aspiration and biopsy were repeated and the results showed acute leukemia with 39% blast cells. Whole-genome sequencing analysis of the patient confirmed the presence of (exon 1; 496 > C-T) non-sense mutation leading to a truncated FANCF protein attributed to a stop codon at the amino acid position 166. Conclusion The study reported the presence of a homozygous C-T exon 1 mutation in FANCF gene in the female pediatric patient from Odisha, India associated with FA. Furthermore, both parents were found to be carriers of FANCF gene mutation, as this allele was found to be in heterozygous state upon genome sequencing. The pathogenicity of the agent was robustly supported by the clinical phenotype and biochemical observations, wherein the patient eventually developed acute myeloid leukemia. The findings of the study infer the importance of early detection of FA and the associated mutations, which might lead to the development of acute myeloid leukemia.