Disclosing an In-Frame Deletion of the Titin Gene as the Possible Predisposing Factor of Anthracycline-Induced Cardiomyopathy: A Case Report

Abstract

Anthracycline-induced cardiomyopathy has been noted as a non-neglectable issue in the field of clinical oncology. Remarkable progress has been achieved in searching for inherited susceptible genetic deficits underlying anthracycline cardiotoxicity in the past several years. In this case report, we present the preliminary results of a genetic study in a young male patient who was treated with standard dose anthracycline-based chemotherapy for his acute myeloid leukemia and attacked by acute congestive heart failure after just two courses of therapy. After a survey of 76 target genes, an in-frame deletion of the titin gene was recognized as the most possible genetic defect responsible for his cardiomyopathy caused by anthracycline. This defect proved to pass down from the patient′s mother and did not exist in seven unrelated chemotherapy-treated cancer patients without chemotherapy-induced cardiomyopathy and four other healthy volunteer DNA donors.

1. Introduction

Tremendous development in the field of anticancer therapy has led to a remarkably improved prognosis of cancer patients worldwide in the past three decades. Nevertheless, those life-saving therapeutic agents are not without adverse effects. Among them, cardiovascular toxicity becomes a peculiar concern with a variety of emergent presentations including myocardial ischemia, hypertension, cardiomyopathy, chest pain, pericarditis, hypotension, and arrythmia [1,2]. Chemotherapy-related cardiomyopathy (CCM) is currently classified into two types: type one, the permanent damage type, is mainly caused by chemotherapeutic drugs such as doxorubicin, daunorubicin, epirubicin, idarubicin, mitoxantrone, and cyclophosphamide, while type two, the reversible damage type, is strongly associated with monoclonal antibody trastuzumab and protein kinase inhibitors such as sunitinib and lapatinib [3]. Most of the cardiotoxic type one agents belong to the anthracycline group, which has a lifetime cumulative-dose relationship with the risk of cardiac failure. The mechanism of anthracycline-induced cardiotoxicity is proposed to be DNA double-strand break, the decreased expression of antioxidative enzymes, and impaired electron transport chains resulting from anthracycline binding with topoisomerase 2β, leading to the death of cardiac myocytes, production of reactive oxygen species, and mitochondrial dysfunction [3,4].

Although risk factors of anthracycline-induced cardiotoxicity have been demonstrated to include cumulative dose, very young or old age, female sex, prior cardiac diseases, existing cardiovascular threatening items, and concomitant treatment with trastuzumab, recent studies revealed an association between underlying genetic variants and anthracycline cardiotoxicity [5]. Due to the limited efficacy of present cardioprotective agents, for example, dexrazoxane, angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, and beta-blockers [6], prophylactic strategies for anthracycline cardiotoxicity have appealed to the use of prediction models and the precedent screening of associated pharmacogenetic variants for cancer patients who are to receive anthracycline therapy [7,8]. Herein, we present a young man with severe heart failure after taking just two courses of anthracycline-based chemotherapy for his acute myeloid leukemia and report the preliminary results of investigating possible underlying predisposing defects in his genome.

2. Materials and Methods

Next-generation sequencing (NGS) and data analysis.

The patient accepted our proposal that a survey of his genome for detecting probable genetic variants related to anthracycline cardiomyopathy might contribute a lot to medicine. After he signed his informed consent and the project was approved by our cooperative Institutional Review Board (IRB number: TYGH109047), his peripheral blood mononuclear cells (PBMCs) were sampled for genomic DNA extraction. Subsequently, NGS was used to establish the whole exome sequences (WES) by Genomics BioSci & Tech. (New Taipei City, Taiwan). The methodology was based on Agilent SureSelect system exome capture and sequencing protocol. The vcf files of WES data archived from Genomics Inc. were uploaded to QIAGEN Clinical Insight Interpret (QCII, QCI^TM, QIAGEN, Hilden, Germany) [9]. After reading and aligning the WES data to human reference genome sequence (hg19), QCII software automatically calls sequence variants and generates a computed report based on the population frequency filter (excluding >1% gnomAD in the East Asian population). To interpret the relationship between the gene variants and pathogenic consequences, we used the specific terms based on the guidance of the American College of Medical Genetics and Genomics (ACMG), including “pathogenic”, “likely pathogenic”, “uncertain significance”, “likely benign”, and “benign” to describe the phenotypes which may be caused by target gene variants [10]. For the data visualization approach, Integrative Genomics Viewer (IGV) was used to generate the genomic mapping graph [11].

We focused on 76 target genes for a comparison analysis, according to the previously published literature. These targets cover most of the genes in which meaningful variants had been frequently detected in patients or experimental animal models with anthracycline-related cardiotoxicity [12,13,14,15]. A total of 76 target genes are listed in

Table 1. Targets genes studied in this project.

Gene	Ensembl Gene ID
ABCB1	ENSG00000085563
ABCC9	ENSG00000069431
ACTA1	ENSG00000143632
ACTN2	ENSG00000077522
ANK2	ENSG00000145362
ANKRD1	ENSG00000148677
ATP1A2	ENSG00000018625
BAG3	ENSG00000151929
CACNA2D2	ENSG00000007402
CASQ2	ENSG00000118729
CAT	ENSG00000121691
CELF4	ENSG00000101489
CORIN	ENSG00000145244
CRYAB	ENSG00000109846
DES	ENSG00000175084
DSP	ENSG00000096696
ERBB3	ENSG00000065361
FLNC	ENSG00000128591
ILK	ENSG00000166333
KCNH2	ENSG00000055118
KCNQ1	ENSG00000053918
LAMA4	ENSG00000112769
LDB3	ENSG00000122367
MIB2	ENSG00000197530
MYH6	ENSG00000197616
MYH7	ENSG00000092054
MYL10	ENSG00000106436
MYL5	ENSG00000215375
MYL6B	ENSG00000196465
MYL7	ENSG00000106631
MYLK	ENSG00000065534
MYLK4	ENSG00000145949
MYLKP1	ENSG00000228868
MYO10	ENSG00000145555
MYO16	ENSG00000041515
MYO1A	ENSG00000166866
MYO1G	ENSG00000136286
MYO1H	ENSG00000174527
MYO3A	ENSG00000095777
MYO3B	ENSG00000071909
MYO5BP1	ENSG00000235130
MYO5BP2	ENSG00000238245
MYO6	ENSG00000196586
MYO7A	ENSG00000137474
MYO7B	ENSG00000169994
MYOF	ENSG00000138119
MYOG	ENSG00000122180
MYOM2	ENSG00000036448
MYOM3	ENSG00000142661
MYPN	ENSG00000138347
MYRF	ENSG00000124920
MYRFL	ENSG00000166268
MYSM1	ENSG00000162601
MYT1L	ENSG00000186487
NEBL	ENSG00000078114
NEXN	ENSG00000162614
NRAP	ENSG00000197893
PKP2	ENSG00000057294
PRDM16	ENSG00000142611
PRKAG2	ENSG00000106617
RAC2	ENSG00000128340
RARG	ENSG00000172819
RBM20	ENSG00000203867
RYR2	ENSG00000198626
SCN5A	ENSG00000183873
SGCD	ENSG00000170624
SLC22A16	ENSG00000004809
SLC28A3	ENSG00000197506
TGFBI	ENSG00000120708
TMEM43	ENSG00000170876
TMPO	ENSG00000120802
TNN	ENSG00000120332
TNNI1	ENSG00000159173
TNNT2	ENSG00000118194
TNNT3	ENSG00000130595
TTN	ENSG00000155657

.

3. Case Presentation

A 20-year-old man was diagnosed as having acute myeloid leukemia with chromosome changes as del (9) (q22) and +10 at a medical center in Taipei city in February 2017. He was treated with two consecutive courses of chemotherapy with standard doses of cytarabine (200 mg/m²/day for 7 days) plus daunorubicin (45 mg/m²/day for 3 days). Complete remission was achieved but, unfortunately, severe congestive heart failure developed soon after the second course of chemotherapy. His left ventricular ejection fraction fell to 11% initially and recovered to 34% after intensive cardiologic care using a combination regimen composed of bisoprolol, valsartan/sacubitril, ivabradine, and spironolactone. Like many other leukemia and cancer patients in Taiwan, he did not take upfront dexrazoxane as a cardioprotective agent along with systemic chemotherapy. Although he had not received further therapy for his leukemia, the disease did not relapse when he attended our hospital for a routine medical follow-up study in February 2020. At that time, an echocardiogram showed that he had a dilated left ventricular chamber with an ejection fraction calculated at around 45%, showing much improvement from the previous estimation. His electrocardiogram showed a normal sinus rhythm without abnormal patterns. The hemoglobin level (15.5 g/dL) and platelet count (151,000/µL) were within reference ranges. There was a mild leukopenia (3600/µL) with an adequate differential distribution (neutrophil 66.4%, lymphocyte 22.1%, monocyte 8.7%, eosinophil 2.5%, and basophil 0.3%).

Based on the WES analysis with QCII, a preliminary data analysis on this case revealed a total of 319 variants related to the 76 target genes described above. After excluding >1% gnomAD in the East Asian population (benign polymorphism) through the population frequency filter provided by QCII, we concluded that three individual gene mutations, TTN, MYO1A, and RYR2, were found to be worth investigation (

Table 2. Alterations of cardiac disease in the CCM case.

Gene	Alteration	Function	Impact	Population Frequency (East Asia, gnomAD)	Pathogenicity 1
MYO1A	c.1630C > T p.R544W	Normal	Missense	0.17%	Uncertain significance
TTN	c.55637_55639delAAG p.E18546del	Loss	In-frame deletion	0.05%	Uncertain significance
RYR2	c.9336T > C p.I3112I	Normal	Synonymous	0.006%	Likely benign

¹ QCII interprets the pathogenicity based on the computed points: pathogenic (above 0.98 points); likely pathogenic (0.90 to 0.98 points); variants of unknown significance (VUS, −0.89 to 0.89 points); likely benign (−0.90 to −0.98 points); benign (Below −0.98 points). Determination of pathogenicity referred to the criteria adapted mainly from the 2016 ACMG/AMP guidelines for germline sequence variant interpretation.

). A further study obtained from the QCII computed database indicated that only TTN variants contributed abnormal phenotypes—YO1A and RYR2 were classified to be normal functional variants. Despite this, a total of 60 variation sites were detected on the TTN gene which encodes titin, a major component of sarcomere in cardiac muscle. Among them, an in-frame deletion, TTN: c.55637_55639delAAG, which led to the loss of a glutamic acid, turned out to be the most likely meaningful TTN gene variation of our CCM index patient (Figure 1). Furthermore, the QCII evidence base referred the Human Gene Mutation Database (HGMD^®) and presented insight findings, depicting TTN variants significantly associated with cardiomyopathy; for example, the TTN missense mutation (c.7060C > T) with the R2354C substitution was validated as the pathogenic variant in hypertrophic cardiomyopathy [16]. Moreover, as reported in a cohort study including pathogenic variants and variants of unknown significance (VUS), increased variant burden was reported to be associated with dilated cardiomyopathy (DCM) [17]. Altogether, although the novel TTN variant was classified to be of uncertain significance in pathogenicity, the QCII knowledge base contains strong evidence to compute and predict the association between this TTN deleterious variation and hypertrophic cardiomyopathy.

The WES data were read and aligned to the hg19 reference genome. The visualization view of genomic mapping showed that AAG in-frame deletion occurred in the TTN gene of CCM case (TAIT-CCM-00), which caused the non-translation of glutamic acid (E) and, finally, altered the amino acid sequence.

The patient′s parents and elder brother, seven unrelated cancer patients (colon cancer—five, breast cancer—one, aggressive lymphoma—one), and four healthy volunteers were included in the extended phase of study after they gave their written informed consent (

Table 3. The information of enrolled volunteers in the present study.

Case No.	Sex	Diagnosis	Anthracycline	CCM
TAIT-CCM-00	Male	AML	+	+
TAIT-CCM-01 (CCM parents)	Male	Health donor	_	_
TAIT-CCM-02 (CCM parents)	Female	Health donor	_	_
TAIT-CCM-03 (CCM parents)	Male	Health donor	_	_
TAIT-CCM-04	Female	Health donor	_	_
TAIT-CCM-05	Female	Health donor	_	_
TAIT-CCM-06	Female	Health donor	_	_
TAIT-CCM-07	Male	Health donor	_	_
TAIT-CCM-08 (DNA QC fail)	Male	Colon cancer	_	_
TAIT-CCM-09	Female	Colon cancer	_	_
TAIT-CCM-10	Female	Colon cancer	_	_
TAIT-CCM-11	Male	Colon cancer	_	_
TAIT-CCM-12	Female	Breast cancer	_	_
TAIT-CCM-13	Male	Lymphoma	+	_
TAIT-CCM-14	Female	Colon cancer	_	_

“+” depicts the patient receiving the Anthracycline therapy or displaying CCM syndrome.

). No cardiomyopathy developed in any of the cancer patients who had all taken systemic chemotherapy without concurrent cardioprotectant dexrazoxane for their diseases. Of note, when comparing to the CCM patient with TTN in-frame deletion, we found that the lymphoma case (TAIT-CCM-13, see

Table 4. QCII computed results of TTN gene.

Case No.	Alteration	Function	Impact	Population Frequency (East Asia, gnomAD)	Pathogenicity
TAIT-CCM-00	c.55637_55639delAAG p.E18546del	Loss	In-frame deletion	0.05%	Uncertain significance
TAIT-CCM-01	No alteration	-	-	_	_
TAIT-CCM-02	c.55637_55639delAAG p.E18546del	Loss	In-frame deletion	0.05%	Uncertain significance
TAIT-CCM-03	c.55637_55639delAAG p.E18546del	Loss	In-frame deletion	0.05%	Uncertain significance
TAIT-CCM-04	No alteration	-	-	_	_
TAIT-CCM-05	c.65504A > G p.N21835S	Loss	Missense	0.44%	Uncertain significance
TAIT-CCM-06	No alteration	-	-	_	_
TAIT-CCM-07	c.13250G > A p.S4417N	Loss	Missense	0.10%	Uncertain significance
	c.23008G > A p.D7670N	Loss	Missense	0.006%	Uncertain significance
TAIT-CCM-09	No alteration	-	-	_	_
TAIT-CCM-10	c.27596G > A p.R9199H	Loss	Missense	0.50%	Likely benign
	c.37143T > C p.A12381A	Normal	Synonymous	0.06%	Likely benign
	c.58211C > G p.S19404C	Loss	Missense	0.54%	Likely benign
TAIT-CCM-11	c.17618T > C p.V5873A	Normal	Missense	0.20%	Uncertain significance
TAIT-CCM-12	c.36157C > T p.R12053W	Loss	Missense	0.15%	Likely benign
TAIT-CCM-13	c.34081C > T p.L11361F	Normal	Missense	0.10%	Likely benign
TAIT-CCM-14	c.1709C > T p.A570V	Normal	Missense	0.74%	Likely benign

) with normal functional TTN alteration had no significant cardiomyopathy after receiving anthracycline therapy. Furthermore, some TTN loss function variants detected in different cancers remained low risk for cardiomyopathy after non-anthracycline chemotherapy in the analysis. WES was established from their genomic DNA and went through the same analytic process as described above, with one colon cancer patient′s DNA sample failing to pass quality control (unique patient number TAIT-CCM-08) and thirteen WES sets, in addition to the patient′s completed the analysis. The final results do suggest that the in-frame deletion TTN variant (TTN: c.55637_55639delAAG) with an alternative phenotype might be a highly possible causing factor for anthracycline-derived CCM.

The in-frame deletion TTN: c.55637_55639delAAG detected in the patient was also disclosed to exist in his mother and elder brother, thus, proving it to be a maternal-side inheritance. This mutation of interest could not be found in the patient′s father and all the other unrelated DNA donors. Nevertheless, few variant alternative TTN mutations identified to be of uncertain significance or likely benign in the QCII analysis were revealed in different DNA donors without cardiomyopathy besides the index patient (Table 4).

4. Discussion

Recent progress in the molecular pathophysiology study of hypertrophic and dilated cardiomyopathy has found meaningful deficits of genes involved in sarcomere composition and function [18]. Genetic deficits in hypertrophic cardiomyopathy result in important conformation changes which interfere with relaxation and energy preservation, leading to dilated cardiomyopathy. It has been revealed that a prevalence of truncating variants of titin, encoded by TTN, leads to a contractile dysfunction of sarcomere [19]. A survey of underlying genetic variants of anthracycline-induced cardiotoxicity was performed, according to results discovered in research on inherited cardiomyopathy disorders. Despite this, we did not detect the same truncating or missense defects of titin previously reported by other groups in our patient [12,13]. The in-frame deletion TTN: c.55637_55639delAAG inherited from the patient′s mother is considered to be the most likely pathogenic mutation underlying the patient′s CCM. To our knowledge, this is the first time that a specific TTN in-frame deletion (c.55637_55639delAAG) is reported to be associated with anthracycline-related CCM. In contrast, another lymphoma patient with a normal TTN missense variant (c.34081C > T) did not have anthracycline-related CCM after treatment with anthracycline-containing regimen.

The molecular mechanisms of CCM are very complex. According to previous studies, the potential causes responsible for CCM might compose of genetic variations relating to metabolism, oxidative stress, inflammation, apoptosis, and autophagy, in addition to structural components in cardiac muscle [20]. We correlate the first-hand clinical findings with the novel TTN deleterious mutation and expect that these results can aid in predicting the toxicity of chemotherapy and provide a new view of the research field. Nonetheless, some limitations remain in this study. First, GRCh38 (hg38) is updated from GRCh37 (hg19) to serve as the human reference genome in 2013 [21]. However, due to the foundation referred by the QCII and in-house cohort in the present study, we still used the hg19 reference genome to align the sequencing reads. Second, it is difficult to survey all the possible candidate genes listed in the literature, but our study has included the most CCM-associated 76 genes reported so far. Third, further investigation is needed to confirm the molecular pathway of the newly detected TTN in-frame deletion in the CCM pathogenesis. Finally, although we have a significant finding that the specific region deletion (c.55637_55639delAAG) detected in the TTN gene profile altered the amino acid sequence (p.E18546del) with a loss-of-function phenotype, more control cases are probably needed to comprehensively demonstrate the pathogenic role of this specific TTN variant in chemotherapy-derived CCM.

5. Conclusions

Altogether, we are glad to find a likely TTN mutation leading to the susceptibility of anthracycline cardiotoxicity in this patient. It is hoped that this finding can contribute valuable information to the field of CCM research, and we plan to conduct more investigations in the near future.