Joint quantitative measurement of hTERT mRNA in both peripheral blood and circulating tumor cells of patients with nasopharyngeal carcinoma and its clinical significance

The study was approved by the Ethics Committee of our institute. All patients and their family members signed the informed consent form. Patients’ medical records were anonymous. 33 (16 male and 17 female) NPC patients diagnosed as undifferentiated squamous cell carcinoma at M0 at the Otolaryngology Development of Southern Medical University Zhujiang Hospital were enrolled in the study. They were at age of 23–70 years old with median age of 49 and staged according to the 2008 Clinical Staging System of NPC [ 15]. Among them, 4 were at stage I, 5 at stage II, 17 at stage III, 7 at stage IV, 11 at stage T1, 6 at stage T2, 13 at stage T3, 3 at stage T4,4 at stage N0, 5 at stage N1, 17 at stage N2, and 7 at stage N3. Patients at stages I and II were subjected to intensity modulated radiation therapy (IMRT) and patients at stages III and IV were subjected to two courses of induction chemotherapy followed by IMRT. Before treatment, after induction chemotherapy and after IMRT, 2 ml of peripheral blood was collected from each patient between 6:00 am to 9:00 pm. In addition, 24 non-cancer inpatients of the Otolaryngology Development of Southern Medical University Zhujiang Hospital were used as controls. For plasma isolation, peripheral blood of each patient and control subject was collected in an anticoagulated tube containing EDTA and centrifuged at 2000 rpm for 10 min within 2 h. The obtained plasma was stored at −80 °C. For CTCs isolation, peripheral blood was placed in a tube without EDTA, mixed with lymphocyte separation medium within 2 h, and centrifuged at 2500 rpm for 20 min. The obtained monocyte layer, which contains CTCs, was collected, washed with PBS and stored at −80 °C.

Trizol was from Invitrogen; PrimeScript RT reagent Kit and SYBR Premix Ex TaqII kit were from Takara; ABI7500 fluorescence quantitative PCR instrument was from ABI, USA; Ficoll-Hypaque lymphocyte separation medium was from Tianjin TCD.

Primer sets for internal control β-actin (5′-TGACACCTCACCTCACCCAC-3′ and 5′-CACTGTCTTCCGCAAGTTCAC-3′) and primer sets for hTERT (5′-CGGAAGAGTGTCTGGAGCAA-3′ and 5′-GGATGAAGCGGAGTCTGGA-3′) were designed using Primer express and synthesized by Sangon Biotech (Shanghai) Co., Ltd.

Two hundred fifty microliter of plasma was mixed thoroughly with 750 μL of Trizol and used for RNA extraction as described by the manufacturer. Total RNA concentration was measured using a UV spectrophotometer and RNA quality was determined by the ratio of absorbance at 260 nm and 280 nm. RNA samples with ratio of absorbance at 260 nm and 280 nm between 1.8 and 2.0 were considered to have high purity and stored at −80 °C for future use.

A total of 1 μg RNA of each sample was used for RT-PCR. cDNA was synthesized by reverse transcription as described by the manufacturer and amplified in a 20 μl of reaction system containing 10 μl of SYBR premix, 0.4 μl of each primer, 0.4 μl of ROX reference Dye II and 0.1 μl of cDNA template at the following reaction conditions: initial denaturation at 95 °C for 30s followed by 40 cycles of 95 °C for 15 s, 60 °C for 20s and 72 °C for 34 s. The melting curve of PCR was analyzed. The experiment was repeated three times and β-actin was used as an internal reference. Relative expression of hTERT to β-actin was calculated using 2 ^-△△Ct.

Peripheral hTERT mRNA content and hTERT mRNA level in peripheral CTCs of NPC patients were used to draw scatter plot and subjected to correlation analysis to obtain Pearson correlation coefficient. The results showed that all data were distributed near a straight line from the lower left to the upper right corner (Fig. 1) and had a Pearson coefficient of 0.981, showing a high correlation.

As we all know, telomerase as well as its catalytic subunit hTERT are closely related with the occurrence and development of vast majority of malignant tumors including NPC. Others and we [ 12, 16] have shown that telomerase was overexpressed in tumor tissues and tumor cell lines, but not in normal tissues and cells. However, the detection of telomerase activity in tumor tissues of patients who has been diagnosed is not helpful for early diagnosis of tumor. Directly detection of telomerase activity from peripheral blood may play an important role in early diagnosis of patients who has not been diagnosed by the naked eyes and microscopy. Miura et al. [ 17] detected hTERT mRNA in peripheral blood of liver cancer patients at early stage and compared it with other serological tumor markers AFP and DCP. Their results showed that serum hTERT mRNA content was higher in liver cancer patients than in patients with chronic liver diseases, but was not related with liver cancer differentiation level. The authors believed that hTERT mRNA in peripheral blood was superior in HCC diagnosis compared with AFP mRNA, AFP and DCP. In addition, they found that serum hTERT mRNA level was significantly different in different tissues and could be used as a new and useful biomarker for cancer. March et al. [ 18] also detected plasma hTERT mRNA content in 49 patients with prostate cancer and found plasma hTERT mRNA content was significantly higher in patients with locally advanced lesions than in patients with localized lesions. Thus, it can be used as a non-invasive marker of prostate cancer to differentiate patients with locally advanced disease at molecular level. Kang [ 7] and March-Villalba et al. [ 19] detected peripheral hTERT mRNA content in patients with gastric and prostate cancer, respectively. Their results showed that hTERT mRNA content in these cancer patients was higher than that in control subjects. They further found that hTERT mRNA content in peripheral blood of patients with gastric and prostate cancer was also closely associated with clinicopathological parameters such as clinical stage, lymph node infiltration range, etc., but not with age and gender. Our study showed for the first time that hTERT mRNA level in peripheral blood of NPC patients was higher than that in control subjects, and was also significantly correlated with patients’ clinical stage, tumor size and lymph node infiltration scope ( P < 0.05). In addition, our results further showed that hTERT mRNA level in peripheral blood of NPC patients at early stage was markedly increased, and this increase became more obvious with severity of tumor stage: the later the stage (for both N and T staging systems) was, the higher the peripheral blood hTERT mRNA content, suggesting that this serological marker could have significance in early diagnosis and clinical staging severity assessment of NPC patients. Our results are consistent with the findings of other scholars on different cancer patients [ 6, 20– 23].

Combined detection of hTERT mRNA with other diagnostic techniques showed a potentially significant value in improving the accuracy of tumor diagnosis and evaluating treatment efficacy of malignant tumors. Ping et al. [ 24] found that plasma hTERT mRNA detection combined with PDG-PET/CT can improve the accuracy of tumor diagnosis. Salvatore et al. [ 25] reported that for colorectal cancer patients receiving neoadjuvant chemotherapy, peripheral hTERT mRNA can be used to assess the efficacy of chemotherapy. Lu et al. [ 26] also showed that peripheral hTERT mRNA level in patients with acute myelogenous leukemia after first chemotherapy decreased to the level of 2.4 ± 2.0 at complete remission from that of 13.5 ± 8.5 before the first treatment ( P < 0.001). Among them, most had normal hTERT mRNA level of 1.2 ± 0.8. Changes in peripheral hTERT mRNA content can also be used to assess the results of tumor surgery. Lu et al. [ 26] reported that the content of hTERT mRNA in peripheral blood of patients with laryngeal squamous cell carcinoma after surgery significantly reduced to 8.0 ± 5.7 from that of 11.8 ± 8.3 before surgery ( P = 0.03), suggesting that peripheral hTERT mRNA may become an important indicator for observation of therapeutic responses of cancer patients.

Our results also showed that peripheral hTERT mRNA content of NPC patients at late stage (III and IV) reached 12.68 ± 3.08 before combined therapy, and was reduced to 10.68 ± 2.48 and 3.13 ± 1.69, respectively, after inductive chemotherapy as well as concurrent IMRT and chemotherapy. It can be seen from the results that after inductive chemotherapy, peripheral hTERT mRNA level was decreased slightly in most patients, while after concurrent IMRT and chemotherapy, hTERT mRNA level was significantly decreased in almost all patients. Moreover, after IMRT, hTERT mRNA level was decreased from 5.60 ± 2.33 to 3.43 ± 1.42 in NPC patients at early stages (I and II). All these results suggested that IMRT or concurrent IMRT and chemotherapy had more obvious impacts on peripheral hTERT mRNA level than induction chemotherapy, suggesting that NPC may be more sensitive to radiation therapy. In addition, the action duration of radiation therapy was also longer than that of chemotherapy, leading to more obvious inhibition of telomerase activity and tumor micrometastasis via blood in NPC patients, thereby affecting peripheral hTERT mRNA content. These results in turn support clinical treatment modalities of radiotherapy supplemented by chemotherapy for NPC patients [ 27].

The fact that examination of peripheral CTCs of cancer patients becomes a hot spot of research shows the importance of this examination. CTCs detection is considered as an important indicator of tumor diagnosis, distal micrometastasis, treatment efficacy monitoring and prognosis. However, due to the heterogeneity and rarity of CTCs, the use of a single marker is generally challenged with lower specificity and sensitivity. Because of the difficulty of selecting individual CTC, studies including ours [ 9] usually use peripheral monocyte layer as material for CTCs. Currently, most researchers use multiple genetic markers to identify peripheral CTCs with one marker positive considered as CTC positive [ 28]. The detection of hTERT mRNA in peripheral CTCs is equally important as detection of hTERT mRNA in peripheral blood for understanding the source of hTERT mRNA and early diagnosis of cancer. Wang et al. [ 29] used multiple markers including hTERT mRNA for detecting CTCs and found that 69.2% of blood samples of breast cancer patients were positive to at least one cancer-associated genetic marker and after completion of treatment, CTCs positive rate dropped to 20.6%.

Our study showed for the first time that hTERT mRNA level in peripheral CTCs was 10.65 ± 4.28, significantly higher than that in control subjects, and significantly correlated with clinical stage, tumor infiltration scope and lymph node metastasis. These results were similar to that in peripheral blood. Even in early stage NPC patients, hTERT mRNA in peripheral CTCs was also increased, and this increase became more obvious with the progress of clinical stage.

Increased peripheral CTCs and hTERT mRNA level are likely new evidences for distal micrometastasis. Cheng et al. [ 8] screened CTCs in peripheral blood and found CTCs count in peripheral blood was correlated with bone metastasis of lung cancer. For NPC patients, distal metastasis to bone, lung, liver or multiple organs is one of the main causes for treatment failure [ 30]. Timely detection of CTCs in peripheral blood and hTERT mRNA content may provide clinical assistance for determination of factors related to tumor recurrence and micrometastasis as well as early intervention of patients with metastasis. In this study, all included 33 patients with newly diagnosed NPC had no distal metastasis. Therefore, it is necessary to conduct controlled prospective study with a large sample size to clarify its relationship with distal metastasis and micrometastasis of NPC, and provide a new reference index for early diagnosis and treatment of NPC.

In this study, we for the first time simultaneously examined hTERT mRNA content in both peripheral blood and peripheral CTCs of NPC patients. The results showed that they increased consistently and appeared to have significant correlation, thus could be used as new serum biological indicators for early diagnosis of NPC. In addition, the results also showed that they were closely related to tumor clinical stage, size and lymph node infiltration scope as well as other clinicopathological factors, and reduced after radiotherapy and chemotherapy, suggesting that joint detection of these indicators could serve as one of the indicators for NPC progression, early peripheral micrometastasis, treatment efficacy and prognosis. These results also laid a foundation for further exploration of the source of peripheral hTERT mRNA and its underlying mechanism.