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Expressions of miR-30c and let-7a are inversely correlated with HMGA2 expression in squamous cell carcinoma of the vulva

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Oncotarget. 2016; 7:85058-85062. https://doi.org/10.18632/oncotarget.13187

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Antonio Agostini, _ Marta Brunetti, Ben Davidson, Claes G. Trope, Sverre Heim, Ioannis Panagopoulos, Francesca Micci

Abstract

Antonio Agostini1,2, Marta Brunetti1,2, Ben Davidson3,4, Claes G. Trope5, Sverre Heim1,2,4, Ioannis Panagopoulos1,2, Francesca Micci1,2

1Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway

2Centre for Cancer Biomedicine, University of Oslo, Oslo, Norway

3Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway

4Faculty of Medicine, University of Oslo, Oslo, Norway

5Department of Gynecology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway

Correspondence to:

Francesca Micci, email: francesca.micci@labmed.uio.no

Keywords: HMGA2, miR-30c, let-7a, FHIT

Received: September 14, 2016     Accepted: October 22, 2016     Published: November 07, 2016

ABSTRACT

Malignant tumors of the vulva, most of them squamous cell carcinomas, account for only 5% of cancers of the female genital tract. Though little is known about the genetic features of these tumors, the Fragile Histidine Triad (FHIT) and High Mobility Group AT-hook 2 (HMGA2) genes were found deregulated. We wanted to gain more knowledge about the expression of HMGA2-related miRNAs such as miR-30c and let-7a, and whether a correlation exists between the expression of FHIT and HMGA2, in this tumor type. An inverse correlation was found in-as-much as HMGA2 was highly expressed (mean fold change 8.8) whereas miR30c and let-7a were both downregulated (mean fold change -3.9 and -2.3, respectively). The consistent overexpression of HMGA2 found in all tumors adds to the likelihood that this gene is of importance in SCC pathogenesis. Moreover, we came to the conclusion that miRNAs may be the cause of the deregulation of HMGA2. Our results also show that SCC of the vulva presents a characteristic molecular pattern with FHIT being downregulated whereas HMGA2 is upregulated.


Expressions of miR-30c and let-7a are inversely correlated with HMGA2 expression in squamous cell carcinoma of the vulva | Agostini | Oncotarget

INTRODUCTION

Squamous cell carcinomas (SCC) account for 70% of all malignant tumors arising in the vulva. [1]. Little is known about the genetic features of this cancer as only 44 cases of vulvar SCC have been cytogenetically and/or molecularly analyzed [26]. Our group has previously reported a chromosome- and array-based comparative genomic hybridization (CGH) analysis of vulvar SCC which showed, among other imbalances, frequent loss of chromosomal band 3p14 [2]. The Fragile Histidine Triad (FHIT) tumor suppressor gene, which maps to this band, was found downregulated [2]. Recently, we showed expression of the High mobility group AT-hook 2 gene (HMGA2) in 86% (20 out of 23) of vulvar SCC analyzed [7].

An inverse correlation between the expression of FHIT, miR-30c, and HMGA2 was found by Suh et al. [6] in lung cancer. FHIT enhances the expression of miR-30c as well as HMGA2 repression thereby inhibiting epithelial-mesenchymal transition and the metastatic process in small cell carcinoma of the lung. The interaction between this miRNA and the HMGA2 3’untranslated region (3’UTR) seems to be crucial in gene expression control [8]. Since our previous findings in SCC of the vulva [2] hint at a similar expression correlation as that detected in lung cancer, we decided to quantify the expression levels of HMGA2 and miR-30c in the 10 tumors of the vulva that were found to have deregulated HMGA2 and FHIT, and to assess the expression levels of the miRNA let-7a which is known to target and repress HMGA2 [911], as well as the expression of the let-7a regulators LIN28A and LIN28B [12].

RESULTS

All molecular investigations gave informative results (Table 1) which were normalized using the two normal vulva tissue samples. HMGA2 was expressed at high levels in all 10 tumors analyzed with an 8.8 fold change average (range: 7-14) (Figure 1A). miR-30c was strongly downregulated in all 10 tumors (Figure 1B) with an average fold change of -3.9 (range: -2.3 to -5.5). The analysis of let-7a expression found downregulation in all cases with a mean -2.3 fold change (range: -0.5 to -3.5) (Figure 1). LIN28A was found deregulated in four out of ten tumors. In these samples, the detected fold changes were -1.5 for cases 1 and 2, - 3.5 for case 3, and -1 for case 10 with a mean fold change of -1.8. Three tumors (cases 4, 7, and 9) showed upregulation of LIN28A with a fold change of 2.5 for case 4, 6 for case 7, and 1.5 for case 9 giving a mean fold change of 3.3. In the remaining three tumors (cases 5, 6, and 8), LIN28A expression was similar to that of the normal controls (Figure 1A). No expression of LIN28B was detected in the 10 SCC of the vulva or in the two normal controls. However, the gene was found expressed in the Total Human Universal Reference used as an internal control for each reaction.

Table 1: Overview of the samples and results

Case/Lab Number

Diagnosisa

FHIT

miR-30c

LIN28A

LIN28Bd

Let-7a

HMGA2

1/02-167

SCC m

-

2/02-848

SCC m

-

3/02-869

SCC h, m, p

-

4/02-1171

SCC

-

5/03-830

SCC m

nec

-

6/03-1011

SCC h, m

nec

-

7/03-1088

SCC h

loss 3p14b*

-

8/06-19

SCC p

nec

-

9/06-125

SCC m

loss 3p14b

-

10/09-733

SCC h

loss 3p14b

-

Arrows are used to show deregulation of the genes (arrow head up: up regulation; arrow head down: down regulation)

a h: highly differentiated, m: moderately differentiated, p: poorly differentiated.

b Genomic Imbalances assessed with an array based Comparative Genomic Hybridization (aCGH) showing a loss of the FHIT locus. * aCGH detected a homozigous deletion for the FHIT locus.

c ne: normal expression (no differences between samples and the normal controls expression levels).

d No LIN28B expression was found in our samples.

Expression profile of the 10 SCC of the vulva.

Figure 1: Expression profile of the 10 SCC of the vulva. A. Relative normalized expression of HMGA2 and LIN28A. B. Relative normalized expression of miR-30c and let-7a.

Searching for possible causes behind the deregulation of let-7a and miR-30c in vulvar SCC, we checked the genomic imbalance charts of these tumors to find if the miRNA clusters for let-7a and miR-30c were deleted. These data were retrived from our previous publication on the very same samples in which an array Comparative Genomic Hybridization study was described [2], looking specifically for the three genes expressing let-7a, MIRLET7A1 on 9q22.3, MIRLET7A2 on 11q24.1, and MIRLET7A3 on 22q13.3, and the two genes for miR-30c, MIR30C1 and MIR30C2, mapping on 1p34.2 and 6q13, respectively. No genomic loss was found for the chromosomal bands in which these miRNAs clusters are located, the only exception being case 10, where a deletion was found in the chromosome arms containing all three MIRLET7A genes (6q, 9q, and 22q).

DISCUSSION

Few SCC of the vulva have been characterized both at the cytogenetic and molecular level. HMGA2 is one of the few genes found to be activated in this tumor type [6]; however, no previous study has quantified its expression. We found that HMGA2 was expressed at high levels in all 10 vulvar SCC analyzed with an average fold change of 8.8. HMGA2 belongs to the High-mobility group AT-hook family of non-histone proteins involved in a wide variety of cellular processes from DNA damage repair to gene regulation [13]. The gene is expressed during embryonic development [14] but is usually unexpressed in adult normal tissues [15]. High expression levels of HMGA2 have been found in various types of tumors including benign connective tissue neoplasms and malignant tumors [16]. HMGA2 promotes diverse tumorigenic processes from cellular proliferation to epithelial-mesenchymal transition (EMT) and metastasis formation [17]. The mechanisms that lead to unchecked expression of HMGA2 in cancer are still not fully understood, but miRNA-dependent regulation seems to play a role. The HMGA2 3’untranslated region (3’UTR) contains regulatory sequences that are targeted by different families of miRNAs [8], and miRNA-dependent repression seems to be the main mechanism to ensure negative HMGA2 expression [10, 11, 18]. Another piece of evidence testifying to the importance of the interaction between HMGA2 and miRNAs is the high frequency of disrupted forms of this gene, due to rearrangement of chromosomal band 12q15, found in different tumors [19]. These alterations bring about loss of the 3’UTR leading to a truncated transcript that evades miRNA-dependent gene silencing [19]. Interestingly, no truncated form of the gene was found in the investigated samples [6], further hinting at the importance of alternative mechanisms of gene deregulation in vulvar SCC. To test this further, we decided to assess the expression of two miRNAs, miR-30c and let-7a, that are known to target and regulate HMGA2 [9, 18].

Downregulation of miR-30c was found in all cases analyzed. For the first time in SCC of the vulva, we showed an inverse correlation betrween miR-30c and HMGA2 expression similar to the one previously reported in lung cancer [18]. Moreover, when retrieving data on FHIT expression from our previous publication [2], we saw similar downregulation of FHIT and miR-30c, admittedly with one sample (case 6) showing a high expression of FHIT in spite of miR-30c downregulation. This indicates that even other causes of miR-30c downregulation may exist in vulvar SCC.

We found downregulation of let-7a in all tumors analyzed. Deregulation of the let-7 family of miRNAs occurs in different types of tumors and the most important result of it seems to be HMGA2 overexpression [20, 21]. This is also the case for SCC of the vulva, where deregulation of HMGA2 could be brought on by altered expression of FHIT, miR-30c, and/or let-7a. Allegedly, deregulation of the let-7 family of miRNA is caused by overexpression of the RNA-binding protein homologues LIN28A and LIN28B that inhibit the maturation of both pri-let-7 and pre-let-7 [12]. Since only three out of ten tumors had overexpression of LIN28A, we conclude that LIN28A is not the primary cause of let-7a downregulation in SCC of the vulva. The correlation between let-7a downregulation and HMGA2 overexpression was previously found also in SCC of the oral cavity [22] and esophagus [23]. These findings strengthen our interpretation and lead us to assume that miRNA deregulation is the major cause of the high HMGA2 expression levels in SCC of the vulva, possibly in squamous cell carcinomas generally.

Our study showed that SCC of the vulva presents a characteristic molecular signature in that FHIT is downregulated while HMGA2 is upregulated. The deregulation of these genes may be correlated with the invasive capacity of these tumors as shown in lung cancer [18]. FHIT is a suppressor gene with a role in apoptosis and epithelial-mesenchymal transition (EMT) [24, 25]. HMGA2 induces EMT and invasiveness in epithelial tumors and high expression levels of the gene have been seen in primary as well as metastatic carcinomas [26]. HMGA2 enhances the TGFβ-SMADs signaling pathway [27] and so upregulates the major transcription factors involved in EMT, i.e, SNAIL1, SNAIL2, and TWIST. The consistent overexpression of HMGA2 found in 10 out of 10 tumors adds to the likelihood that this gene is of general importance in SCC pathogenesis. MiRNAs may be the cause of the HMGA2 deregulation. This irrespective, the deregulation of these genes together with downregulation of FHIT constitutes a molecular signature of vulvar SCC.

MATERIALS AND METHODS

Tumor material

The material consisted of fresh frozen samples from 10 SCC of the vulva and two normal vulva specimens surgically removed at The Norwegian Radium Hospital (Table 1). The tumors have previously been examined for chromosomal aberrations and genomic imbalances as well as for expression of FHIT [2, 4] and HMGA2 [6]. The study was approved by the regional ethics committee (Regional komité for medisinsk forskningsetikk Sør-Øst, Norge, http://helseforskning.etikkom.no) and written informed consent was obtained from the patients.

Total RNA extraction

Total RNA was extracted using the miRNeasy Kit (Qiagen, Hilden, Germany) and QIAcube (Qiagen) according to the manufacturers’ recommendations. RNA concentration and purity was measured using a Nanovue Spectrophotometer (GE Healthcare, Pittsburgh, PA, USA).

Real-time polymerase chain reaction (real-time PCR)

The expression of the target miRNAs and genes was assessed with Real-Time PCR. The PCR analyses were performed using the CFX96 Touch Real-Time PCR detection system (Bio-Rad Laboratories, Oslo, Norway). The reactions were carried out in quadruplicate using the TaqMan Universal Master Mix II with UNG (Applied Biosystems, Foster City, CA, USA) following the manufacturer’s protocol. Human Universal Reference Total RNA (Clontech, Mountain View, CA, USA) was used as internal reaction control with two samples of normal vulva tissue being used for normalization.

MicroRNA expression

Ten ng of total RNA were reverse transcribed with the TaqMan MicroRNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. miRNA expression was assessed with Real-Time PCR using the TaqMan MicroRNA Assays (Applied Biosystems) for let-7a (TM:000377) and miR-30c (TM:000419). The RNU6B gene (TM:001093) was used as a reference.

Gene expression

One μg of extracted total RNA was reverse-transcribed in a 20 μl reaction volume using iScript Advanced cDNA Synthesis Kit according to the manufacturer's instructions (Bio-Rad Laboratories, Oslo, Norway). Gene expression was assessed with Real-Time PCR using the TaqMan Gene Expression Assays (Applied Biosystems): HMGA2 (Hs_04397751_m1), FHIT (Hs_00179987_m1), LIN28A (Hs_00702808_s1), LIN28B (Hs_01013729_m1), and ACTB (Hs_01939407_gH). The latter gene was used as a reference.

ACKNOWLEDGMENTS

This work was supported by grants from the Norwegian Radium Hospital Foundation.

COMPETING INTEREST

The authors have no competing interest to disclose.

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