Skip to main content

01.12.2017 | Case report | Ausgabe 1/2017 Open Access

BMC Cancer 1/2017

Tracking the origin of simultaneous endometrial and ovarian cancer by next-generation sequencing – a case report

BMC Cancer > Ausgabe 1/2017
Nadejda Valtcheva, Franziska M. Lang, Aurelia Noske, Eleftherios P. Samartzis, Anna-Maria Schmidt, Elisa Bellini, Daniel Fink, Holger Moch, Markus Rechsteiner, Konstantin J. Dedes, Peter J. Wild
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​s12885-017-3054-6) contains supplementary material, which is available to authorized users.
Computer tomography
Oestrogen receptor
Formalin fixed paraffin Embedded
Fédération internationale de gynécologie Obstétrique
Mismatch repair
Microsatellite stable
Next-generation sequencing
Progesterone receptor
Progesterone receptor
The cancer genome atlas


Endometrioid adenocarcinoma of the uterus and ovarian endometrioid carcinoma share many morphological and molecular features [ 1, 2]. Coincidence of both primary tumours is a relatively common event which occurs in about 10% of patients with ovarian carcinoma and in about 5% with endometrial carcinoma [ 3]. When simultaneous uterine and ovarian carcinomas show the same histology and differentiation, determination of the primary origin may be difficult. In case of independent primary tumours, this might be due to the several common risk factors shared by the two malignancies or due to germline alterations that predispose to the development of simultaneous cancers. In most cases, however, one of the endometrioid type carcinomas is the primary tumour that gives rise to a metastatic lesion. It is also not excluded that both carcinomas might originate from a common endometrial epithelial precursor cell of origin, a theory that can explain the histological and genetic similarities of the lesions [ 4]. Distinguishing between two independent lesions versus one primary and one metastatic lesion is extremely difficult, nevertheless important for the prognosis and treatment of the patient [ 5].
A novel powerful tool to identify common genetic alterations specific for a cancer entity and to provide information on the tumour clonal evolution is next-generation sequencing (NGS) [ 6]. To date, the knowledge of the mutational landscape of many different tumours including endometrial and ovarian cancer has increased throughout the last 10 years. TCGA has published data from whole exome sequencing of a large number of both gynaecological malignancies [ 1, 2]. Furthermore, studies have been reported on endometrial and ovarian carcinoma using two different cohorts – one including patients with endometrial endometrioid carcinomas and one consisting of ovarian endometrioid carcinomas [ 4]. The authors suggest that although the same genes are affected in both cancers the mutation patterns differ possibly due to the different microenvironment in the ovary and the uterus. This offers a possibility to determine the origin of simultaneously identified endometrial and ovarian endometrioid lesions. While these reports contribute to the big picture of what are the most common aberrations in the corresponding tumour type and beyond doubt profit from the large number of cases investigated, single patients with synchronously diagnosed endometrial and ovarian cancer can shed light on the direct tumour evolution. Although NGS is broadly used in preclinical research, thus providing the possibility to unravel genetic alterations and potential therapeutic targets, in the clinical setting current diagnostics and treatment of metastatic endometrial and ovarian cancer is still mainly based on radiological and conventional histological results as well as chemotherapy combination regimens.
In the present case report we investigated the mutation pattern in a 33-year-old female patient diagnosed with synchronous endometrioid adenocarcinoma of the corpus uteri and the left ovary. The patient developed a lung metastasis of an endometrioid type adenocarcinoma four years after laparoscopic hysterectomy, vaginal brachytherapy and tibolon therapy. Based on histological findings, it is difficult to decide whether the gynaecological carcinomas are two independent primary carcinomas occurring in parallel. Furthermore, it is almost impossible to recognize the origin of the lung mass. Thus, we employed targeted NGS of 409 tumour-related genes (Ion Ampliseq Comprehensive Cancer Panel, Thermo Fisher) in order to identify the relation between the two carcinomas and the source of the distant metastasis. Moreover, we were interested in the genetic fingerprint of the metastasis to clarify the recurrence-free survival of the patient after its removal and megestrol treatment for seven years. Finally, we looked for possible germline mutations from blood samples of the patient that could explain the early onset of the disease.


Clinical history and pathological findings

A 33-year-old woman, who has undergone a diagnostic curettage due to hypermenorrhoea and menorrhagia, was diagnosed with endometrial endometrioid adenocarcinoma of moderate differentiation and with squamous components. Subsequently, a laparoscopic hysterectomy with pelvic washing, bilateral adnexectomy and pelvic lymphadenectomy was performed. In the hysterectomy, well-differentiated residual cancer was found with infiltration less than one half of the myometrium, consistent with stage pT1a.
The tumour tissue showed high expression of oestrogen and progesterone receptors (both 100%, Fig.  3). Unexpectedly, a synchronous well differentiated endometrioid adenocarcinoma with squamous components of the left ovary was detected. The tumour mass was confined to the ovary according to stage pT1a. The contralateral ovary showed no pathological alterations. All pelvic lymph nodes ( n = 20) were free of tumour. In summary, the former pathological TNM classification for the corpus uteri was pT1a pN0 (0/20) G2 (FIGO stage IA) and for the ovary pT1a pN0 G1 (FIGO stage IA). Vaginal brachytherapy of 4x5 Gy was administered because of a G2 tumour and the quite young age of the patient. After treatment with tibolon (2.5 mg/day) for 4 years, the patient presented with chest pain in the right upper thorax. Through CT-scan and the following thoracoscopic resection of the right upper lobe of the lung, a metastatic endometrioid adenocarcinoma was removed. Treatment with megestrol (160 mg/day) was started. In addition to the clinical check-up, a CT-scan was performed each year. The latest PET–CT scan after 7 years being treated with megestrol acetate showed no evidence of tumour recurrence. Informed consent was obtained and the study has been approved by the local ethics committee (KEK-ZH-No. 2010–0358).

Immunohistochemical analysis

Tumour tissue sections were immunohistochemically investigated with the following antibodies: oestrogen receptor (SP1 Ventana-Roche, prediluted), progesterone receptor (1E2, Ventana-Roche, prediluted), mismatch repair proteins as MSH2 (25D12, Novocastra Lab Ltd., 1:100), MSH6 (BD Biosciences 1:500), MLH1 (G168-15, PharMingen Becton Dickinson 1:100), PMS2 PharMingen BD 1:300), PTEN (6H2.1 DAKO, 1:200), beta-Catenin (14/beta-Catenin, BD Biosciences, 1:50), ARID1A/BAF250a (HPA005456, Sigma Chemicals, 1:200), and γH2AX (Novus Biologicals, 1:1200).
After antigen retrieval, the slides were incubated with the primary antibodies. After incubation for 1 h at room temperature, the staining of ER, PR, beta-Catenin, and γH2AX was further conducted with the Ventana Benchmark automated system (Ventana Medical Systems, USA) using Ventana reagents such as UltraView HRP (for ER, PR), UltraMap™ DAB detection kit for γH2AX, and Optiview (beta-Catenin). The antibodies against the mismatch repair proteins and ARID1A were incubated for 30 min and the staining procedure was carried out with the automated Leica BOND system using the Bond Polymer Refine Detection Kit (Leica Biosystems).

DNA extraction

Histological slides from FFPE tissue specimens were reviewed for tumour content and the tumour area was marked by a trained gynaecopathologist for tissue punching (Fig.  2). DNA from peripheral blood and FFPE punches (3 cylinders with diameter of 0.6 mm) was isolated with the Maxwell 16 LEV Blood DNA kit (Promega, #AS1290) and Maxwell 16 FFPE Tissue LEV DNA Purification Kit (Promega, #AS1130), respectively, according to the manufacturer’s recommendations. Briefly, 300 μl of blood collected in a BD Vacutainer K2 (EDTA 18.0 mg) tube was added to 30 μl of Proteinase K solution (final concentration 2 mg/ml) and subsequently mixed with 300 μl lysis buffer, vortexed and incubated for 20 min at 56 °C. FFPE cylinders were deparaffinised with xylene, washed twice with ethanol, dried 10 min at 37 °C and resuspended in 200 μl incubation buffer containing 2 mg/ml Proteinase K. Samples were incubated overnight at 70 °C and mixed with 400 μl lysis buffer. Lysates from both, blood and FFPE tissue were transferred to well 1 of the supplied cartridge of the corresponding kit and DNA was automatically purified and eluted in 30 μl Tris-buffer, pH 8.0 by the Maxwell instrument.

Next generation sequencing (NGS)

Targeted NGS of 409 cancer related genes was performed with 40 ng DNA using the Ion AmpliSeq Comprehensive Cancer Panel (Thermo Fisher Scientific) according to the manufacturer’s protocol. Alignment, variant calling and filtering were performed with Ion Reporter 4.4 (Thermo Fisher Scientific). The following filter chain was used: “Location in utr_3, splicesite_3, exonic, splicesite_5, utr_5” in, “variant effect in stoploss, nonsense, missense, frameshiftInsertion notframeshiftInsertion, nonframeshiftBlockSubstitution, frameshiftDeletion, nonframeshiftDeletion, frameshiftBlockSubstitution” in, “USCS Common SNPs” not in, allele ratio between 0.05 and 1.0 in, allele read-count between 100 and 100 000 in, variant type “INDEL, LONGDEL, SNV, MNV” in. Variants selected after visual inspection of the reads in IGV that displayed more than 15% variant frequency were verified with Sanger sequencing (Additional file 1: Table S1).

Sanger sequencing

Primers were designed to amplify 200 bp fragments surrounding the position of the detected variant (Additional file 1: Table S1). PCR products were purified and subjected to Sanger sequencing in two reactions, one with the forward and one with the reverse primer.


Histopathological considerations

Histopathological evaluation of the simultaneous endometrial and (unilateral) ovarian cancer as well as the lung metastasis revealed the same tumour morphology, showing an endometrioid adenocarcinoma with low grade features and squamous components (Fig.  1). Squamous differentiation is a common feature of endometrioid type cancer and may occur in both endometrial and ovarian tumours. Precursor lesions like endometrial hyperplasia or components of an ovarian borderline-tumour or endometriosis were not identified.
In summary, the endometrial and ovarian neoplasms showed the very same histomorphology and differentiation, and no precursor lesions were found, neither in the ovary, nor in the uterus. The primary site of cancer origin, however, could not be clarified with this observation. To further address this key question we first compared the size of the lesions. Since the endometrial carcinoma was larger than the ovarian tumour, the uterus is in favour of the primary origin. However, a common or multifocal origin can also be hypothesized.

Genetic alterations (NGS)

To gain insight into the tumour biology we used targeted deep re-sequencing. DNA was extracted from the tumour area and the correct excision of the FFPE punches was confirmed with HE staining (Additional file 2: Figure S1). 409 genes were re-sequenced with the Ion AmpliSeq Comprehensive Cancer Panel (Thermo Fisher Scientific). Variants present in the blood were excluded (the full table of variants from two technical replicates are listed in Additional file 1: Table S2) and the variants of interest with a frequency of more than 15% were verified with Sanger sequencing (Additional file 2: Figure S2 and data not shown). The variant frequency in each sample was determined as percent variant reads from total reads.
Somatic mutations in ARID1A, RAF1, CTNNB1, PIK3CA, ESR1, SYNE1, PIK3CG PTEN, PTPRT and USP9X were detected (Table  1, Fig.  2a). PhyloP, SIFT, Grantham, PolyPhen are different algorithms predicting the damage caused by a mutation and at least one of them suggested impaired protein function arising from all listed mutations. Furthermore, the SNVs in CTNNB1, PIK3CA, PTEN and ESR1 were annotated in COSMIC, the catalogue of somatic mutations in cancer.
Table 1
Mutations, identified with NGS
Mutation type
Ref - > seq
Blood [%]
EmCa [%]
OvCa [%]
Meta [%]
Amino Acid Change
chr1: 27094447
A- > AT
chr3: 12641248
CA- > C
chr3: 41266125
c.122C > T
2.8 0.86 2.26
COSM5730; COSM5701; COSM5676; COSM29289
chr3: 178936095
A- > G
c.1637A > G
COSM767; COSM12459; COSM25041
chr6: 152419923
A- > G
c.1610A > G
COSM1074637 COSM1074639
chr6: 152443737
C- > A
c.26228G > T
chr7: 106524631
C- > G
c.2792C > G
chr10: 89692790
T- > A
c.274G > T
COSM86049; COSM50762; COSM3566
chr10: 89692886
T- > A
c.370 T > A
2.41 1.95
COSM5224; COSM5824; COSM1577271; COSM921089
chr10: 89692892
G- > A
c.376G > A
COSM5051; COSM5211; COSM28889
chr20: 40710566
C- > T
c.4285G > A
chrX: 41057832
A- > C
c.4432A > C
* PhyloP score:• Positive scores -- Measure conservation, which is slower evolution than expected, at sites that are predicted to be conserved; • Negative scores -- Measure acceleration, which is faster evolution than expected, at sites that are predicted to be fast-evolving
** SIFT score: • 0.0–0.05 - deleterious; • 0.05–1.0 – tolerated
*** Grantham score: Higher Grantham scores are considered more deleterious
****PolyPhen-2 score: • 0.0–0.15 -- Variants with scores in this range are predicted to be benign; • 0.15–1.0 -- Variants with scores in this range are possibly damaging; • 0.85–1.0 -- Variants with scores in this range are more confidently predicted to be damaging
Interestingly, SNVs in PTEN (p.Cys124Ser and p.Ala126Thr) and PTPRT (p.Val1429Met), and one-base indels in RAF1 (p.Met350fs) and ARID1A (p.Arg1053fs) were shared by the endometrial and ovarian carcinomas but not found in the lung metastasis. On the other hand, the lung metastasis carried mutations in ESR1 (p.Tyr537Cys) and PTEN (p.Asp92Tyr) that were not detected in the endometrial and ovarian carcinomas. USP9X (p.Met1478Leu) was mutated only in the ovarian adenocarcinoma. In contrast, PIK3CG (p.Ser931Cys) was altered only in the endometrial adenocarcinoma.
The general distribution of the detected mutations showed that most of them (8/12) are shared by the endometrial and ovarian tumour. Only a single private mutation in the ovarian and endometrial lesion was found (Fig.  2b). Three of eight mutations were also detected in the lung metastasis, although with lower frequencies (Fig.  2a and b). Further, the lung metastasis had acquired two additional mutations.

Protein expression profile (immunohistochemistry)

The immunohistochemical profile was consistent in all three cancer manifestations. The hormone receptor expression was strong in almost 100% of tumour nuclei. The expression of four mismatch repair proteins (MSH2, MLH1, MSH6, PMS2) was visible in normal and tumour tissue, suggestive of microsatellite stable (MSS) carcinomas (Fig.  3). Expression of PTEN, beta-Catenin, and ARID1A was observed in all tumour samples (Fig.  4). γH2AX staining was used as a surrogate marker for double strand breaks. Nuclear γH2AX expression was observed in single cells of the ovarian tumour but less in the endometrial and metastatic tumour. Interestingly, the expression was found not only in the glandular tumour component but also in the squamous part (data not shown).


In the present study, we investigated the molecular profile of a simultaneous low-grade endometrioid endometrial and ovarian carcinoma as well as of a lung metastasis in a young female patient. From the histology alone, the primary origin is sometimes difficult to determine. The identification of precursor lesions, the pattern of spread and tumour size are valuable parameters for this differentiation. Immunohistochemical analysis of hormone receptors, PTEN and beta-Catenin may show overlapping staining patterns and is therefore not always helpful. The simultaneous occurrence of an endometrial and ovarian carcinoma in women below 50 years of age is a common combination [ 3], however, the pattern of pulmonary metastasis in this low grade and low stage cancer disease is unusual.
In our molecular analysis, we detected and verified mutations in genes such as ARID1A, CTNNB1, PIK3CA, and PTEN which are frequently affected in these tumour entities [ 7, 8]. However, no striking alterations in mismatch repair genes known to cause early development of endometrial cancer were detected.
We further showed that some mutations were lost during the metastasis formation, either due to the treatment or because of redundancy with other alterations affecting the same pathway. Last but not least, we identified enrichment of mutations causing upregulation of PI3K signalling that could explain the prolonged complete remission under megestrol acetate.
Somatic mutations were identified with targeted PCR-based NGS and verified with Sanger sequencing. The fact that 67% (8/12) of the detected alterations were shared by the ovarian and endometrial tumour with similar variant frequencies suggests a common origin of the two lesions. PTEN is more frequently mutated in low-grade endometrial endometrioid carcinomas (67%) compared to low-grade ovarian endometrioid carcinomas (17%). In contrast, CTNNB1 mutations are significantly different in low-grade ovarian endometrioid carcinomas (53%) compared to 28% of the low-grade endometrial endometrioid carcinomas [ 4]. In the present case, both genes were mutated in both tumours, hampering the unambiguous identification of the primary lesion. However, all shared mutations showed a slightly higher variant frequency in the endometrial adenocarcinoma. Based on this observation it is tempting to speculate that the endometrial adenocarcinoma gave rise to the ovarian adenocarcinoma. The clones that populated the ovary seemed to be of mixed origin and the cells containing the mentioned mutations could have lost their selection advantage in the ovarian microenvironment. The origin of the lung metastasis, however, could not be specified unambiguously.
The early onset of the malignant disease in this young woman at age 33 suggests possible germline mutations that accelerated the accumulation of genetic aberrations promoting cancer development. A common genetic defect that leads to the development of endometrial cancer in the context of Lynch syndrome is aberrations in the mismatch repair (MMR) proteins. Interestingly, neither mutations in the MMR genes nor increased double strand breaks could be detected. Another possible cause of the early disease onset is Cowden’s syndrome. Targeted PCR-based re-sequencing, however, is not the ideal method to detect large gene deletions. The uniformity blot (sequencing depth across amplicons) for the PTEN gene showed no inconsistencies. Therefore, larger deletions on chromosome 10 were unlikely. In addition, germline PTEN mutations could be ruled out.
The one base insertion detected in gene ARID1A causes a frame shift at codon 1053 of the protein. Since the percentage of the mutation suggested a heterozygous alteration, the sustained immunohistochemical staining is probably due to wild-type ARID1A expressed in the tumour samples. However, our study does not provide information on the expression status of the mutated protein or possible dominant negative interference with wild-type ARID1A. The mutation was not present in the metastasis or present at a low percentage from a marginal subclone indicating that this mutation was not substantially contributing to the tumour spread.
In contrast, the somatic mutations in CTNNB1 and PIK3CA were detected not only in the endometrial and ovarian tumours, but also in the lung metastasis. Both mutations are reported in COSMIC, providing experimental evidence that both mutations affect the function of the each protein and are pathogenic. The amino acid change p.Thr41Ile caused by the SNV c.122C > T in CTNNB1 increases protein stability of beta-catenin and leads to its relocalisation to the nucleus [ 9]. The SNV c.1637A > G in PIK3CA results in a mutant PI3K displaying increased substrate phosphorylation [ 10]. Hyperactivation of the PI3K pathway is a known cancer driving event in endometrial cancer [ 8].
Another key protein that is a part of the same signalling cascade and was affected by gene mutations in the described case is the tumour suppressor PTEN. The PTEN SNV c.370 T > A results in replacement of the cysteine in the active site against serine (p.C124S) leading to an enzymatically inactive protein. Although, as shown by immunohistochemistry, the protein level was not affected and the mutation was likely to be heterozygous, it has been recently reported that this enzymatically dead mutant inhibits wild-type PTEN in a dominant negative manner [ 11]. Additionally, we found a second PTEN mutation (c.376G > A) that leads to a threonine replacing the alanine at the adjacent position 126 of the protein, likely to distort the tertiary structure of the active site. None of the PTEN mutations could be detected in the lung metastasis. Instead, another PTEN mutation (p.Asp92Tyr) was detected in the lung metastasis that is also annotated in COSMIC. A possible explanation for the loss of the dominant negative PTEN mutation is the biological redundancy of the PTEN inactivating and PIK3CA activating mutations that both lead to an elevated signalling through the PI3K pathway. Indeed, there is evidence that single clones from the primary tumour are able to colonise distant organs and that the metastases carry rather less mutations than the primary tumour due to natural selection process that sustains only the aberrations indispensable for tumour cell survival and proliferation [ 12]. Interestingly, four years after surgery the patient presented with a lung metastasis that was excised and a therapy with megestrol acetate was initialised. To date, the patient is recurrence-free. Megestrol acetate is reported to act through de-phosphorylation of the PI3K downstream target Akt [ 13], which might be a possible reason for the complete response of the patient to the treatment.
It has been shown very recently by two independent groups that a majority of synchronous endometrial and ovarian endometrioid carcinomas show clear evidence of clonality [ 14, 15]. The findings of these two studies strongly indicate that a considerable part of clinically synchronous endometrial and ovarian endometrioid carcinomas constitute in fact dissemination from one site to the other which is also very likely in our case. In our study we extend these results by next generation sequencing analysis of a distant metastasis and demonstrated that not all mutations found in the primary tumour were conserved in the metastasis. This is illustrated e.g. by the SNVs in PTEN (p.Cys124Ser and p.Ala126Thr) and ARID1A (p.Arg1053fs) which were found in both, the endometrial and the ovarian endometrioid carcinoma, but were not conserved in the distant lung metastasis. Co-occurrence of mutations in ARID1A and PTEN have been shown as potential cancer driving mutations in endometrioid ovarian carcinomas in animal models [ 16]. Interestingly, these two mutations were not conserved in the distant metastasis, indicating another clonal event. Neither the PTEN nor the ARID1A mutation has given rise to the distant metastasis. To our knowledge this is the first case demonstrating the lack of an ARID1A mutation in a distant metastasis of an ARID1A mutated primary tumour. This demonstrates that even very frequent and potential cancer driving mutations such as PTEN and ARID1A in endometrioid endometrial and ovarian cancer may not be found in distant metastases, a fact that is essential for potential future targeted therapies [ 1719]. However, this also demonstrates the importance of sequencing metachronous distant metastases since its mutational profile may differ from the profile of the primary tumour.


In conclusion, our results demonstrate that next generation sequencing is an important tool in the differentiation of simultaneous primary tumours and metastases, which has an important impact for clinical practice. This may not only be valuable information for prognostic considerations, but also may be of increasing importance for future targeted therapies.


The authors wish to acknowledge Annette Bohnert, André Fitsche, Christiane Mittmann, Peter Schraml (Tissue Biobank University Hospital Zurich), Adriana von Teichmann, Peggy Tzscheetzsch, Martina Storz, Fabiola Prutek and Susanne Dettwiler for their technical assistance.


This work was supported by the Krebsliga Schweiz Grant Nr.: KLS-3384-02-2014-R (PJW).

Availability of data and materials

The materials are commercially available. The data is publicly available except for the germline variants of the patient. The patient’s samples are not available due to ethics restrictions.

Authors’ contributions

NV and FL contributed equally to this work. KD and PW share the senior authorship for this work. NV, MR, EB and AN drafted the manuscript, performed the immunohistochemical analysis and the sequencing. FL and ES drafted the manuscript and acquired and interpreted the clinical data. HM drafted parts of the manuscript and interpreted genomic data. PJW and KD participated in the study design, manuscript writing and project coordination. AMS and DF acquired and interpreted the clinical data. All authors have read and approved the final manuscript.

Competing interests

All authors declare no competing financial interests.

Consent for publication

The consent to publish was obtained from all participants.

Ethics approval and consent to participate

The authors confirm that all consent to publish has been obtained in writing from the participants and the study has been approved by the local ethics committee (KEK-ZH-No. 2010–0358).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Über diesen Artikel

Weitere Artikel der Ausgabe 1/2017

BMC Cancer 1/2017 Zur Ausgabe

Neu im Fachgebiet Onkologie

Mail Icon II Newsletter

Bestellen Sie unseren kostenlosen Newsletter Update Onkologie und bleiben Sie gut informiert – ganz bequem per eMail.