Skip to main content
  • Letter to the Editor
  • Open access
  • Published:

CLN5 in heterozygosis may protect against the development of tumors in a VHL patient


Von Hippel-Lindau syndrome (VHL) is a rare disease of dominant inheritance that increases susceptibility to tumor development, with a complete penetrance at the age of 60. In this report, we present the unprecedented case of a VHL carrier who remains healthy at 72. Under the course of this study, it was discovered that this patient carries a mutation for a second rare disease, Neuronal Ceroid Lipofuscinosis (NCL or CNL). We hypothesize that the CLN mutation she carries offers a protective effect, preventing tumor development in the cells potentially suffering a VHL second hit mutation. To test this hypothesis, we ran a series of molecular experiments and confirmed that cell viability of primary endothelial cells decreases upon CLN5 silencing. Our results further elucidate the cell biology implications of two rare diseases interacting.


A rare disease affects, by definition, no more than 1 in 2000 individuals in the European Union [1], and less than 200,000 total in the United States [2]. Although the likelihood of having one rare disease is small, more than 7000 different types have been described, accounting for 30 million patients in Europe alone [3,4,5]. Despite the increasing efforts to investigate rare diseases [6], little is known about families, or patients carriers or suffering more than one rare condition. The co-occurrence/segregation of two independent diseases in consanguineous and non-consanguineous families has been reported in the past [7], but the molecular interaction between the conditions has seldom been investigated. In this case report we present a unique and, to the best of our knowledge, unprecedented combination of two rare diseases segregating in a family, leading to an unexpected clinical picture: a 72 year old woman carrying mutations in heterozygosis for both Neural Ceroid Lipofuscinosis (NCL or CNL) and Von Hippel Lindau disease (VHL), with no development of any pathology.

NCL are a group of neurodegenerative disorders of recessive inheritance, with an incidence as high as 1 in 12,500 births [8]. Currently, fourteen genetically differing forms have been described, corresponding to mutations in different genes (CLN1 to CLN14), and they are all characterized by loss of nerve cells and accumulation of lipopigments within cells. This lysosomal lipid accumulation is due to an inability to degrade lipids, and leads to a neurological atrophy typical of the disease [9, 10]. The patient of this case report is NCL symptom-free, as she is a carrier in heterozygosis for a CLN5 mutation.

The other rare disease in play is VHL, a dominant autosomal disorder affecting 1 in every 36,000 births, characterized by the susceptibility to a series of tumors, typically hemangioblastomas (HB) of the Central Nervous System (CNS) or retina, clear cell renal cell carcinomas (ccRCC) and pheochromocytomas [11]. These develop after a second hit mutation in VHL - a tumor suppressor gene - causes the loss of functional VHL protein [12, 13]. Under normoxic conditions, VHL protein recognizes and binds the previously hydroxylated Hypoxia Inducible Factor (HIF) to trigger its proteasomal degradation [14]. Tissues suffering a stochastic VHL second hit mutation unfold a lack of functional VHL protein, which induces a state of pseudo-hypoxia, promoting tumor growth in these tissues where cells have lost heterozygosis [15].

Despite VHL’s dominant inheritance and almost complete penetrance at the age of 60 [16,17,18], the patient here presented has not shown any VHL symptoms throughout her lifetime. However, her son inherited her mutation and developed bilateral suprarenal tumors in his thirties. Given the family history of two rare diseases, this led us to think of a possible interaction between NCL and VHL. In order to determine the possibility of said interaction, we completed the genetic screening of the patient and her relatives, and performed cellular and molecular assays on primary and established cell lines.

The combination of our in vitro results and the clinical data gathered from the studied family points towards a protective effect by NCL in this patient regarding tumor development: VHL cells that suffer a second hit mutation in VHL cannot divide and progress to develop a tumor, due to the lower viability caused by NCL haplo-insufficiency, interfering in some way with the process of tumorigenesis. These data show a unique counteracting interaction resolving in a symptom-free patient.

Results and discussion

Background: family history

The family here presented came to our attention through our collaboration with the Spanish VHL patient Alliance. The first member of the family to be diagnosed with VHL was subject E (Fig. 1), who presented with bilateral pheochromocytomas at the age of 34. Upon genetic screening of the immediate relatives, it was discovered that subject A carried the same VHL mutation as subject E, and thus had been maternally transmitted to him.

Fig. 1
figure 1

Genetic pedigree of the family of interest showing information on their VHL and CLN5 genotypes and phenotypes (healthy, lipofuscinosis affected or VHL). Circles represent females and squares represent males. The genotype and phenotype of each family member is indicated underneath. Subject A is the subject of interest carrying a VHL mutation and not developing any tumors. Black arrow indicates first family member diagnosed with VHL

Intriguingly, subject A remains completely healthy at the age of 72, despite her VHL mutation. Since her diagnosis, she undergoes annual examinations according to the international follow-up protocol for VHL disease, which includes direct and indirect ophthalmoscopy, MRI of the CNS, abdominal MRI, diagnostic audiologic evaluation and catecholamines tests. No clinical findings of VHL have been found so far, constituting the only known case to the best of our knowledge, of a VHL patient lacking any of the disease symptoms. Taking a closer look at the family’s history, we discovered that patient A had two elder sons who died as teenagers, due to a different rare disease: NCL. Upon learning this, we realized that patient A is carrier of a CLN mutation, in particular at the CLN5 gene.

Altogether, the family’s history suggests that her lack of VHL symptoms can be based on a protective effect that would prevent tumor development. At this point our hypothesis was that this subject’s cells, in case of suffering a VHL second hit mutation normally leading to tumor formation [11, 12], would be no longer viable due to their CLN5 mutation, and thus would not progress into tumor. The next experiments were designed to test this hypothesis.

CLN5 silencing reduces cell viability in different primary and established cell lines

Hemangioblastoma primary cell culture

To test our hypothesis, we started by silencing CLN5 in HB cells from a VHL patient. These cells have already suffered the second hit mutation and thus are VHL (−/−), adequate to test how a CLN5 protein deficiency might affect cell viability in them. In vitro cell cultures showed a significantly reduced number of cells in the CLN5 transfected groups, quantitatively supported by cell counter measurements (Fig. 3a). Next, to assess if apoptosis was promoting cell death in siCLN5 transfected cells, Bax gene expression was quantified by quantitative PCR (qPCR). Bax was chosen for its known involvement in triggering apoptosis [19]. RT-qPCR analysis showed that CLN5 silencing was successful (Fig. 2a), and that the levels of pro-apoptotic gene Bax appeared significantly elevated in the partially CLN5 silenced population (Fig. 2b). These results taken together make us think that CLN5 deficient HB cells have a disadvantage and do not expand at the rate control groups do, since their viability is compromised.

Fig. 2
figure 2

qPCR results in HB primary cells, 72 h after transfection with siCLN5 and siScrambled (siScl). Control group was left untreated, while siScl serves as a negative control. The experiment was conducted in triplicates, representing the mean and showing the standard deviation as error bars. aCLN5 expression; bBax expression. Statistical significance is represented as *p < 0.05; **p < 0.01; and ***p < 0.001

786-O cell culture

As primary cultures of HB are sensitive to the process of transfection by liposomes and were not expanding optimally, we chose to continue with a more resistant VHL (−/−) sample, the human ccRCC 786-O cell line. This time, as a direct measure of cell viability, we quantified ATP levels at different times after CLN5 gene silencing. The reduction in cell viability was best seen at 48 h, with a 20% loss compared to control (Fig. 3b). The concordance between the positive and negative controls shows that the transfection reagent used for silencing (Lipofectamine) does not have a significant effect on cell viability, and therefore, the drop in cell viability in partially silenced CLN5 cells is due only to the decrease of CLN5 transcript levels.

Fig. 3
figure 3

a Cell count by Bio-Rad TC20 Automated Cell Counter. Primary HB cells were trypsinized 72 h after transfection with siCLN5 and siScl as negative control. Cell viability was measured in 786-O cells (b) and ccRCC primary cells (c) 48 h after transduction by a luciferase assay, where ATP levels are a direct correlation of cell viability. d ccRCC primary cell cultures under the microscope were photographed 72 h after transfection. Control group was left untreated, while siScl serves as negative control. Every condition was replicated three times – the graphs show the combined mean of these experiments, representing the obtained standard deviation in the error bars. Statistical significance is represented as *p < 0.05; **p < 0.01; and ***p < 0.001

ccRCC primary cell culture

Although we observed a decrease in cell viability upon CLN5 depletion, this effect might be diluted by the high replicative rate characteristic of a cell line. This is why we chose a second VHL (−/−) primary cell culture, different than HB (which was not expanding optimally): primary ccRCC cells derived from the tumor of a VHL patient. The previous results were successfully replicated – again, a 20% decrease in cell viability is observed in the siCLN5 group, 48 h after transfection (Fig. 3c). This was visually apparent under the microscope; CLN5 silenced cells were less confluent than the control groups (Fig. 3d).

CLN5 protein levels are decreased in endothelial cells derived from VHL patients

Once we established that CLN5 silencing reduces cell viability in VHL (−/−) tumor cells, we wondered whether there is an interaction between CLN5 and VHL, both at transcript and protein levels. We opted for qPCR measurement of CLN5 gene expression, and Western blotting to determine CLN5 protein levels in endothelial cells (ECs) derived either from VHL patients or from healthy donors. These primary culture cells called BOECs (Blood Outgrowth Endothelial Cells) are heterozygous VHL (+/−) in the VHL group, and VHL (+/+) in the control group.

Both techniques indicated reduced levels of CLN5 in the VHL group; qPCR showed a 0,6 fold reduction of CLN5 expression in VHL versus the healthy control (Fig. 4a), and a 20% reduction in CLN5 protein levels in VHL (+/−) ECs, compared to control levels (Fig. 4b). These results suggest a putative interaction between CLN5 and VHL: lower levels of VHL protein seem to correlate with a decrease in CLN5 protein expression. We think that there might be a direct interaction of both proteins VHL and CLN5 in the cell, since both are part of the cell degradative pathways - CLN5 is involved in the lysosomal and VHL in the proteasomal degradation. It is possible that a crosstalk among both pathways up to a functioning threshold level may be necessary. Further protein-interaction in vitro experiments would be necessary to confirm this concept.

Fig. 4
figure 4

aCLN5 expression levels as measured by qPCR. b CLN5 and actin protein expression by Western blot and further quantification. Statistical significance is represented as *p < 0.05; **p < 0.01; and ***p < 0.001

In summary, subject A, introduced in section 1 and who is VHL (+/−) and CLN5 (+/−), would have a roughly 50% deficiency in CLN5 protein due to her heterozygous CLN5 mutation. In addition to this, and according to our in vitro results, because of her VHL mutation, her cells would be further reduced at CLN5 protein levels. As a result, despite the CLN5 heterozygous condition, the real CLN5 levels would be below the 50% expected in a heterozygote. Upon a second hit in VHL, the levels of CLN5 would fall even lower, below a functional threshold, leading to a pseudolipofuscinosis phenotype in cells suffering this second hit. This condition, highly toxic from a metabolic point of view, would not enable cell proliferation and survival. Thus, the cells suffering a VHL second hit mutation will not expand, preventing tumor development. This hypothesis has been supported by an observation made in our lab: BOECs obtained from subject A are not susceptible to VHL silencing. After siRNA VHL transfection, most of the cells die, and the few remaining have no silenced VHL, according to qPCR (data not shown). Overall, our work suggests that a second hit mutation in VHL is incompatible with a CLN5 heterozygosis cellular background. Protective effects of the kind have been previously described in VHL [20], and we propose that this is a similar case, where one mutation suggests the patient to a protection against the disease development.


Cell culture

CNS HB and ccRCC primary cultures from excess of resected surgeries of VHL patients under informed consent were isolated as previously described [21]. HBs, ccRCCs and the human renal cancer cell line 786-O cells (ATCC® CRL-1932™) were all cultured in RPMI supplemented with 20% Fetal Bovine Serum (FBS), 2 mM L-glutamine, and 100 U/mL penicillin/streptomycin (all from GIBCO, Grand Island, NY, USA). All the cellular assays were performed at 37 °C, 5% CO2 and ~ 95% humidity.


Cell transfection assays were performed using Lipofectamine® RNAi MAX Reagent (Thermo Scientific, Rockford, IL, USA), following manufacturer instructions. The following siRNAs were used: Scrambled (#SIC001) from Sigma-Aldrich (Saint Louis, MO, USA) for control, and a combination of 1-CLN5 (#8149), 2-CLN5 (#18061) and 3-CLN5 (#146678) from Ambion/Thermo Scientific for CLN5 silencing. The transfection efficiency was around 75%, as estimated by experiments with fluorescent probes conducted in parallel.

Cell viability assay

The viability of the ccRCC primary cultures and 786-O cell line was measured by the “Luminescent Cell Viability Assay” (Promega, Madison, WI, USA). This is a homogeneous quantitative method to determine the number of viable cells in culture based on quantitation of the ATP presence, which indicates metabolically active cells. Cells were lysed at 48 h or 72 h after transfection as follows: Cell Titer-Glo reagent (Lysis buffer, Ultra-Glo Recombinant Luciferase, Luciferine, and Mg2+) was added to wells to a final proportion of 1:1, and gently mixed for 30 min at room temperature (RT). Next, luminescence was measured in three independent measurements using a Glomax Multidetection System (Promega).

Real-time RT-PCR (qPCR)

Total RNA was extracted from HB cells using Nucleo Spin RNA kit (Macherey-Nagel, Düren, Germany). One microgram of total RNA was reverse-transcribed in a final volume of 20 μl with the First Strand cDNA Synthesis Kit (Roche, Mannheim, Germany) using random primers. SYBR Green PCR system (BioRad, Hercules, CA, USA) was used to carry out real-time PCR with an iQ5 system (BioRad). Primers used for qPCR are: 18S Fwd: 5′-CTCAACACGGGAAACCTCAC- 3′, 18S Rev.: 5′-CGCTCCACCAACTAAGAACG-3′; BAX Fwd: 5′-CACTCCCGCCACAAAGAT-3′, BAX Rev.: 5′-CAAGACCAGGGTGGTTGG-3′; CLN5 Fwd: 5′-AAGCCCCAGTATGGGAATT-3′, CLN5 Rev.: 5′-TGCCAGTTAATGTACTTCTGAATCC-3′.

Western blot

For protein extraction, cells were lysed on ice for 30 min in TNE buffer (50 mM Tris, 150 mM NaCl, 1 mM EDTA, and 0.5% Triton X100) supplemented with wide-range protease inhibitors (Roche, Basel, Switzerland) and lactacystin (Sigma-Aldrich), a specific proteasome inhibitor. Lysates were centrifuged at 14,000×g for 5 min. Similar amounts of protein from cleared cell lysates were boiled in SDS sample buffer and analyzed by 4–20% SDS-PAGE under non-reducing conditions (BioRad). Proteins from gels were electro-transferred to nitrocellulose membranes (Amersham, Little Chalfont, UK) followed by immunodetection with anti-CLN5 (Abnova, Taiwan), and anti-actin (Sigma-Aldrich). Following primary antibody incubation overnight at 4 °C, samples were washed and incubated with the corresponding horseradish peroxidase-conjugated secondary antibodies from Dako (Glostrup, Denmark) at RT for 1 h. All antibodies were used at the dilution recommended by the manufacturer. Membranes were developed by chemiluminescence (SuperSignal West Pico Chemiluminescent Substrate, Thermo Scientific).

Statistical analysis

Results are presented as mean ± SEM. Statistical analyses were performed using the Student’s t-test, comparing siCLN5 results to groups Control and SiScl, independently. Statistical significance was defined when p < 0.05 (*p < 0.05; **p < 0.01, ***p < 0.001).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.



Blood Outgrowth Endothelial Cells


Clear cell Renal Cell Carcinomas


Neuronal Ceroid Lipofuscinosis


Fetal Bovine Serum




Hypoxia inducible factor


Human Umbilical Vein Endothelial Cells


Magnetic Resonance Imaging


Quantitative Polymerase Chain Reaction


Von Hippel Lindau


  1. 2014 Report on the State of the Art of Rare Disease Activities in Europe. EUCERD Joint Action. European Comission. 2019. Accessed 10 Oct 2019.

  2. Genetic and Rare Diseases Information Center. NIH, Gaithersburg, MD. 2019. Accessed 10 Oct 2019.

  3. Rare diseases in numbers: preliminary report from an on going bibliographic study initiated by Eurordis in partnership with Orphanet. Orphanet Rare Disease Platform, Paris. 2018. Accessed 10 Oct 2019.

  4. What Is a Rare Disease? EURORDIS Rare Diseases Europe. Fondation Universitaire, Brussels. 2007. Accessed 10 Oct 2019.

  5. Fanny Cortés DM. Las Enfermedades Raras Rare Diseases. Clínica Las Condes. 2015;26:425–31.

    Google Scholar 

  6. Austin CP, Cutillo CM, Lau LPL, Jonker AH, Rath A, Julkowska D, Thomson D, Terry SF, de Montleau B, Ardigò D, Hivert V, Boycott KM, Baynam G, et al. Future of rare diseases research 2017–2027: an IRDiRC perspective. Clin Transl Sci. 2018;11:21–7.

    Article  Google Scholar 

  7. Lal D, Neubauer BA, Toliat MR, Altmöller J, Thiele H, Nörnberg P, Kamrath C, Schänzer A, Sander T, Hahn A, Nothnagel M. Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing. PLoS One. 2016;11:1–16.

    Google Scholar 

  8. Rider JA, Rider DL. Batten disease: past, present, and future. Am J Med Genet Suppl. 1988;5:21–6.

    Article  CAS  Google Scholar 

  9. Radke J, Stenzel W, Goebel HH. Human NCL neuropathology. Biochim Biophys Acta - Mol Basis Dis. 1852;2015:2262–6.

    Google Scholar 

  10. Mole SE, Cotman SL. Genetics of the neuronal ceroid lipofuscinoses (batten disease). Biochim Biophys Acta - Mol Basis Dis. 1852;2015:2237–41.

    Google Scholar 

  11. Barontini M, Dahia PLM. VHL disease. Best Pract Res Clin Endocrinol Metab. 2010;24:401–13.

    Article  CAS  Google Scholar 

  12. Maher ER, Neumann HPH, Richard S. Von Hippel-Lindau disease: a clinical and scientific review. Eur J Hum Genet. 2011;19:617–23.

    Article  CAS  Google Scholar 

  13. Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER. Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors. Am J Hum Genet. 1997;60:765–71.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Kaelin WG. Molecular basis of the VHL hereditary cancer syndrome. Nat Rev Cancer. 2002;2:673–82.

    Article  CAS  Google Scholar 

  15. Kim WY, Kaelin WG. Role of VHL gene mutation in human cancer. J Clin Oncol. 2004;22:4991–5004.

    Article  CAS  Google Scholar 

  16. Poulsen MLM, Budtz-Jørgensen E, Bisgaard ML. Surveillance in von Hippel-Lindau disease (vHL). Clin Genet. 2010;77:49–59.

    Article  CAS  Google Scholar 

  17. Maher ER, Yates JRW, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA. Clinical features and natural history of von hippel-Lindau disease. Qjm. 1990;77:1151–63.

    Article  CAS  Google Scholar 

  18. Maher ER, Iselius L, ML JRWY, Benjamin C, Harris R, AW JS, NM MAF-S. Von Hippel-Lindau disease: a genetic study. J Med Genet. 1991;28:443–7.

    Article  CAS  Google Scholar 

  19. Basu A, Haldar S. The relationship between BcI2, Bax and p53: consequences for cell cycle progression and cell death. Mol Hum Reprod. 1998;4:1099–109.

    Article  CAS  Google Scholar 

  20. Gascón A, Escobar B, Montero-Conde C, Rodríguez-Antona C, Ruiz-Llorente S, Osorio A, et al. Loss of the actin regulator HSPC300 results in clear cell renal cell carcinoma protection in Von Hippel-Lindau patients. Hum Mutat. 2007;28(6):613–21.

    Article  Google Scholar 

  21. Albiñana V. Villar Gómez De Las Heras K, Serrano-Heras G, Segura T, Perona-Moratalla AB, Mota-Pérez M, De Campos JM, Botella LM. Propranolol reduces viability and induces apoptosis in hemangioblastoma cells from von Hippel-Lindau patients. Orphanet J Rare Dis. 2015;10:1–12.

    Article  Google Scholar 

Download references


We thank the family presented for their participation in this study and providing the details needed to put together this manuscript, the Spanish VHL patient Alliance, and Dr. Martínez-Piñeiro (MD) and Dr. Aguirre (MD) for providing with ccRCC and HB samples respectively. We also thank Dr. Villar Gómez de las Heras (MD) for critically reviewing the manuscript. We acknowledge support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI).


Funding was provided by the projects SAF 2014–52374-R and SAF2017–83351-R from the Ministry of Economy and Competitivity to LMB. The group is part of the CIBER Spanish consortium for Rare Diseases, CIBERER, unit 707, and was also financially supported by the Spanish VHL patient Alliance.

Author information

Authors and Affiliations



L.M.B. designed the complete study. L.M.B., I.R.-P., A.M.C., and V.A. wrote the main manuscript text and figures. All experiments were done by I.R.-P, with technical support of L.R.-P and A.R.R. A.M.C. provided blood samples. All authors critically reviewed the manuscript and approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Corresponding author

Correspondence to Luisa-María Botella.

Ethics declarations

Ethics approval and consent to participate

All methods described in the present manuscript were carried out in accordance with all the international relevant guidelines and regulations of obliged fulfilment in the National Research Council of Spain (CSIC), and in agreement with worldwide regulations for Molecular Research, as also following the guidelines of the Declaration of Helsinki. A written informed consent was obtained from the patients prior to sample collection and publication of this case report.

Consent for publication

All authors critically reviewed the manuscript and approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Rojas-P, I., Albiñana, V., Recio-Poveda, L. et al. CLN5 in heterozygosis may protect against the development of tumors in a VHL patient. Orphanet J Rare Dis 15, 132 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: