Background
Molecular subsets of non-small cell lung cancer (NSCLC) have been defined by various types of driver gene mutations involving epidermal growth factor receptor (
EGFR), v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (
KRAS), and anaplastic lymphoma kinase (ALK) gene fusion. Specific tyrosine kinase inhibitors (TKIs), such as EGFR-TKIs (erlotinib and afatinib) and ALK-TKIs (crizotinib and alectinib), that inhibit the oncogenic activity of these genes have been developed and approved [
1,
2]. A key issue in identifying patients that would be suitable for the targeted agents is precisely identifying the presence or absence of the driver gene mutations in a molecular diagnosis of the lung cancer. In approximately 5% of NSCLC, the rearrangement of the amino-terminal (N-terminal) region of echinoderm microtubule associated protein like 4 (
EML4) with the carboxy-terminal (C-terminal) region of ALK occurs by inversion within the short arm of chromosome 2 [
3]. In cancer cells with
EML4-ALK, the transcription of the C-terminal region of ALK depends on the promoter activity of the fusion partner,
EML4, which is a housekeeping gene for the stabilization of microtubules during mitosis, by which the C-terminal ALK protein level also becomes elevated [
4,
5].
To detect
ALK fusion, there are three different techniques: fluorescence in situ hybridization (FISH), immunohistochemistry (IHC) and reverse transcription–PCR (RT-PCR) are available for the detection of
ALK fusion [
3]. Although each test has some advantages and disadvantages, IHC is more useful as a routine screening method in clinical settings because of cost effectiveness and technical ease [
3]. The ALK IHC method determines whether tumor cells are harboring an
ALK fusion using an antibody directed to the C-terminal ALK protein, but unlike FISH tests, it has been reported to show not only positive results in patients with
ALK fusion–positive cancer but also false-negative errors in some patients who actually have
ALK fusion–positive cancer [
3,
6‐
8]. In addition to
ALK fusion, RET proto-oncogene (
RET) or v-ros UR2 sarcoma virus oncogene homolog 1 (
ROS1) are rearranged in approximately 1% of NSCLC. In consequence, RET-TKIs (such as alectinib or vandetanib) and ROS1-TKIs (such as crizotinib or lorlatinib) are under development for fusion-positive NSCLC patients, and precise diagnostic methods for these fusions are needed [
2,
9‐
11].
In this study, we verified the reliability of IHC methods that target ALK, RET, and ROS1 C-terminal protein as diagnostic tools for lung cancer by investigating whether the expression at the C-terminal region is elevated in each of the fusion-positive lung cancer cells compared with that in fusion-negative cells.
Discussion
Chromosomal rearrangements involving
ALK,
RET, and
ROS1 are attractive anticancer targets that provide opportunities for therapies for patients with NSCLC [
9]. As described in previous preclinical studies [
18,
19], only the three
ALK fusion–positive cell lines in the 12 cell lines tested were sensitive to all ALK-TKIs (alectinib, crizotinib and ceritinib) through the suppression of phosphorylation of ALK signaling pathways involving STAT3/AKT/ERK (Additional file
7: Table S5, Additional file
14: Figure S3, Additional file
13: Figure S9, Additional file
15: Figure S10, and Additional file
16: Figure S11), indicating that the growth of these
ALK fusion–positive cell lines strongly depends on the signal from ALK. In the US, both a FISH test using the Vysis ALK break apart FISH probe kit (Abbott Laboratories) and an IHC test using the Ventana ALK (D5F3) CDx assay (Ventana Medical Systems; Tucson, AZ) have been approved as a companion diagnostic (CDx) test for crizotinib [
20]. In Japan, the Vysis FISH test has been approved as a CDx test for crizotinib, and a diagnostic tool combining the Vysis FISH test with an IHC test using the N-Histofine ALK Detection kit (Nichirei Biosciences) has been approved as a CDx test for alectinib [
6]. These two IHC kits, which respectively include clone D5F3 or 5A4 as a primary antibody directed to C-terminal ALK protein, were highly concordant with the ALK FISH tests. However, it was reported that IHC-positive and FISH-negative patients were occasionally present, with these discordant patients showing a clinical response to crizotinib [
6,
21,
22]. To identify patients who would be suitable for ALK-TKIs, the accurate diagnosis of
ALK fusion is a critical issue. In this study, we focused on the reliability of the detection of C-terminus ALK protein for the diagnosis of
ALK fusion using various types of lung cancer cell lines and tissues. We found that the promoter of
EML4 was constitutively activated in lung cancer as well as normal cells independent of
ALK fusion, and C-terminal ALK protein level and phosphorylation were specifically elevated in
ALK fusion–positive cancer cells (Figs.
2 and
3b). As previously demonstrated [
4,
7], these findings suggest that wild-type ALK is silenced in normal lung cells because of lack of production, but when C-terminal
ALK is fused to N-terminal
EML4 in normal cells, the transcription of the kinase domain of ALK is activated by the constant promoter activity of
EML4, and the resultant abundantly produced EML4-fused ALK leads to cancer through aberrant ALK signal transduction. Therefore, IHC tests for ALK, such as those using the Ventana and N-Histofine kits, could be sufficiently reliable diagnostic methods in the treatment of patients with lung cancer using ALK-TKIs.
As previously described in preclinical studies [
16,
23,
24], 2 cell lines tested only LC-2/ad or HCC78 cell line with
RET or
ROS1 fusion were sensitive to RET-TKI (alectinib) or ROS1-TKIs (crizotinib and ceritinib) by suppressing the level of phosphorylation of STAT3/AKT/ERK, which are located downstream of RET or ROS1 kinase, respectively (Additional file
7: Table S5, Additional file
13: Figure S9a, Additional file
15: Figure S10 and Additional file
16: Figure S11). No IHC or FISH CDx tests that detect
RET or
ROS1 fusions have been approved, but an IHC test using an antibody clone, EPR2871 (Abcam), is under investigation [
10]. Although RET expression was low in normal lung tissue [
25], discordant results between the IHC test and the FISH test for RET have been reported [
26,
27]. In this study, the promoter activity of
KIF5B or
CCDC6, which are two major genes involved in fusion with C-terminal RET, was constitutively activated in every cell line, and the expression of C-terminal RET was considerably high not only in the
RET fusion–positive cell line LC-2/ad, but also in one of the five
RET fusion–negative and
KRAS-mutated cell lines Calu-6. Wild-type RET expression in Calu-6 cells has been also reported by Zhou et al. [
28]. The weight of RET protein in LC-2/ad or Calu-6 cells was, respectively, 50 to 100 kDa or 100 to 200 kDa (Figs.
1b and
2), which is approximately the same weight as that reported previously for, respectively, CCDC6-fused RET or wild-type RET [
29,
30]. Just as surprisingly, in 37 cell lines, phosphorylation of the C-terminal RET domain was only detected in the
RET fusion–negative and
MET-amplified NCI-H1993 cell line (Fig.
2), but that elevation of the level of MET phosphorylation by trans-phosphorylation of MET within RET and MET heterodimers was reported in NCI-H1993 cells [
31]. Both Calu-6 and NCI-H1993 cells were completely insensitive to alectinib (Additional file
7: Table S5 and Additional file
13: Figure S9b and c), which means that cell growth with wild-type RET is independent of RET kinase even if the cells have high expression or high phosphorylation of RET, and RET kinase would be an oncogenic growth driver after fusion with, for example,
CCDC6 or
KIF5B. Taking all these findings together, the stand-alone RET IHC test for the detection of C-terminal RET protein may cause misleading judgments of
RET fusion, and CDx tests with both IHC and FISH or RT-PCR would be needed in the treatment of patients with
RET fusion–positive lung cancer using RET-TKIs.
Regarding the ROS1 IHC test using an antibody for the C-terminus, some patients were reported to show discordant results between IHC and FISH tests despite low expression of ROS1 protein in normal lung tissue [
11,
32]. However, in this study, the
ROS1 fusion–positive cell line, HCC78, harboring an
SLC34A2-ROS1 fusion only showed protein expression at the C-terminal domain and a sensitivity to the ROS1-TKIs by inhibiting ROS1 signaling pathways involving STAT3/AKT/ERK (Figs.
1c and
2 and Additional file
7: Table S5 and Additional file
15: Figure S10).
SLC34A2 and
CD74 are two genes fused to C-terminal
ROS1, and
SLC34A2 mRNA expression was shown in tissues and cell lines of NSCLC as well as normal lung tissues [
33‐
35]. CD74 protein was also strongly expressed in many lung cancer tissues [
36]. Therefore, the C-terminal ROS1 protein level could only be elevated by the strong promoter activity of genes such as
SLC34A2 or
CD74 in
ROS1 fusion–positive lung cancer cells, which suggests that the ROS1 IHC test is a reliable diagnostic test for the detection of patients with lung cancer who have
ROS1 fusion.
On the other hand, ALK or ROS1 IHC tests occasionally showed positive results even in patient samples diagnosed by FISH or RT-PCR tests to be fusion-negative [
6,
8,
11]. As one of the causes of this IHC+/FISH- discordance, it was reported that wild-type FISH signals in fusion–positive cases were caused by rare atypical chromosomal rearrangements with
EML4 and
ALK [
6]. In addition, Takeuchi K et al. showed that ALK expression is detected in some
ALK fusion–negative cases with small-cell carcinoma, large-cell neuroendocrine carcinoma, and poorly differentiated carcinoma [
7]. Hyper-methylation of promoter and copy number gain of
ROS1 were reported as one of the mechanisms that activate ROS1 expression in fusion-negative carcinomas [
37]. However, the possible factors of discordances mentioned above have not been fully clarified at present. This study with 37 lung cancer cell lines and four tissues did not reproduce the phenomenon of discordance. Therefore, further studies using a larger panel with various types of lung cancer cell lines and tissues would be useful to elucidate the causes of discordance in clinical ALK or ROS1 IHC tests.
Next-generation sequencing (NGS) technology enables high-throughput and multiplex analysis of various driver oncogenes. For NSCLC, NGS-based tumor-profiling multiplex gene panels, such as Oncomine Dx target test or FoundationOne CDx, have recently been approved as companion diagnostics to detect mutations of EGFR and BRAF, or fusions of ALK and ROS1 in the US [
38]. These NGS panels are also designed to detect
RET fusions [
39,
40]. At present, clinical diagnosis to select patients with ALK fusion–positive NSCLC is predominantly performed by IHC test, while NGS screening might have the potential to test for multiple gene alterations in a quick single analysis. In this study, we could not compare the analysis of fusions by IHC with that by NGS since we have no data on NGS. However, evaluations of the usability of diagnosis by NGS compared to IHC or FISH in NSCLC specimens showed that NGS screenings could provide an alternative method of detecting fusion genes to IHC or FISH tests [
39‐
41]. Therefore, further studies of NGS in addition to C-terminal protein expression analysis using NSCLC cell lines would be a strong support to precise selection of NSCLC patients with fusion genes by NGS with or without IHC.