NLRC5 expression in tumors and its role as a negative prognostic indicator in stage III non-small-cell lung cancer patients

  • Authors:
    • Xiaoyu Li
    • Fuchun Guo
    • Yongmei Liu
    • Hui‑Jiao Chen
    • Feng Wen
    • Binwen Zou
    • Dan Li
    • Qin Qin
    • Xiaoke Liu
    • Yali Shen
    • Yongsheng Wang
  • View Affiliations

  • Published online on: July 8, 2015     https://doi.org/10.3892/ol.2015.3471
  • Pages: 1533-1540
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Abstract

Major histocompatibility complex (MHC) class I molecules have a crucial role in tumor immune evasion; however, the association of MHC class I molecules with outcomes in cancer patients remains controversial. Nucleotide‑binding oligomerization‑like receptor family caspase recruitment domain‑containing 5 (NLRC5) has been reported to be a MHC class I transactivator. However, the expression and function of NLRC5 in cancer remains to be elucidated. The present study aimed to retrospectively examine NLRC5 expression in human tumor tissues and its association with clinical outcomes of non‑small‑cell lung cancer (NSCLC) stage III patients. The expression of MHC class I and NLRC5 in NSCLC were detected using immunohistochemistry (IHC). The association between their expression levels was assessed using the Pearson's χ2 test and their association with survival was assessed using Kaplan‑Meier analysis and the log‑rank test. In addition, the expression of NLRC5 and MHC class I were examined in 323 cases of seven other types of tumors and their correlations were studied. The results revealed that the expression of NLRC5 was correlated with that of MHC class I in NSCLC patients (P=0.008). MHC class I‑positive and nuclear NLRC5‑positive NSCLC patients were found to have shorter overall survival (OS) rates (log‑rank, P=0.032 and P=0.039, respectively). In addition, in the seven different tumor types, there was a significant correlation between MHC class I and NLRC5 nuclear expression (P<0.001) as well as MHC class I and NLRC5 cytoplasmic expression (P=0.003). In conclusion, NLRC5 was demonstrated to be widely expressed in eight tumor tissues and its expression was correlated with that of MHC class I. Of note, nuclear NLRC5‑negative and MHC class I‑negative stage III NSCLC patients had improved OS rates compared to those with positive expression. Therefore, NLRC5 and MHC class I may be negative prognostic indicators in NSCLC stage III patients.

Introduction

Tumor immune evasion has a critical role in tumorigenesis and progression (1). Major histocompatibility complex (MHC) class I molecules are important for tumor immune evasion due to their function in antigen presentation to T-lymphocytes and cytotoxic T-lymphocytes (CTL) function (2). In addition, the loss of MHC class I is a common mechanism of experimental and spontaneous tumors, which allows them to evade recognition and destruction by CTLs (3,4). In MHC class I downregulated or deficient tumor cells, tumor-associated antigens are not presented to the CTLs, which results in tumor immune evasion and affects the prognosis of tumor patients (3). However, whether MHC class I molecules have a positive or negative role in tumor patients' survival remains controversial. Certain studies have reported that MHC class I loss has poor outcomes due to its impact on antigen presentation to T-lymphocytes and CTLs (5,6). By contrast, other reports have revealed that MHC class I loss may improve patients' survival through activating natural killer (NK) cell function (7,8). These results vary between different types of tumors and the occurrence of lymph node metastasis (5,7).

It has been reported that NLRC5 may have a positive role in the regulation of MHC class I expression in human cell lines and mice models. NLRC5 function was examined in NLRC5-deficient mice, the results of which revealed reduced MHC class I expression in lymphocytes, including T, NK and NKT lymphocytes (9,10). NLRC5 localizes to the nucleus of lymphocytes, where it promotes MHC class I gene expression via stimulation of the H-2D and H-2K gene promoters (11,12). Human NLRC5 is predominantly expressed in hematopoietic cells as well as the spleen, lymph nodes, bone marrow and thymus; in addition, NLRC5 is expressed abundantly in the lungs and intestines (10,11,1318). Staehli et al (10) reported that HeLa cells express NLRC5 when induced by interferon-γ. MHC class I molecules have a critical role in tumor immune evasion and are associated with cancer prognosis; since, NLRC5 was reported to act as a MHC class I transactivator, it may therefore affect tumor patients' survival through regulating tumor immune evasion through MHC class I. Thus, evaluating the expression of NLRC5 in human solid tumors and exploring its association with MHC class I expression and patients' survival may offer a novel method for predicting patient prognosis and provide potential novel therapeutic targets.

The present study aimed to examine NLRC5 expression in human tumor tissues and its association with clinical outcomes of non-small-cell lung cancer (NSCLC) stage III patients. The expression of NLRC5 and MHC class I was determined in non-small-cell lung cancer (NSCLC) stage III tissues and the correlation between NLRC5 (cytoplasmic and nuclear) and MHC class I was analyzed. In addition, the clinical data of NSCLC patients was collected in order to study the association between clinical outcomes and the expression of NLRC5 and MHC class I. Furthermore, the present study aimed to examine the expression of NLRC5 and MHC class I in seven different types of common human solid tumors in tissue microarrays (TMAs) using immunohistochemistry (IHC).

Materials and methods

NSCLC patients

A total of 62 NSCLC patients who underwent radical resection of stage III-node involvement (N)2, without any preoperative therapy, were included in the present retrospective study. All patients were diagnosed and underwent surgery at West China Hospital (Chengdu, China) between January 2001 and September 2003. Histological diagnosis was established according to the guidelines of the World Health Organization (19). Pathological findings, including tumor size, location and lymph node status, were described in the reports of board-certified pathologists. Out of the 62 NSCLC patients, the pathological diagnoses included 31 with adenocarcinoma cell cancer, 24 with squamous cell cancer and 7 with other pathology types. Patients' age at the time of surgery ranged from 26 to 75 years, with a median age of 58 years. Long-term outcome was determined from hospital records and information from follow-up appointments. Overall survival (OS) was measured from the date of surgery to either mortality or the final follow-up visit. Progression-free survival was calculated from the date of surgery to the time of the first local or distant recurrence, or mortality from any cause. Local recurrence was defined as tumor regrowth in hilar, mediastinal, supraclavicular lymph nodes or at the bronchial margin of resection, as visualized using computed tomography (CT) scans. Recurrences beyond those sites were deemed as distant metastases. The present study was approved by the Ethics Committee of Sichuan University (Chengdu, China). Written informed consent was obtained from all patients and all clinical investigations were performed according to the principles of the Declaration of Helsinki.

TMAs

Seven different types of human tumor paraffin-tissues were purchased from the company of Ailina Biotechnology Co., Ltd (Xi'an, China), including 69 renal carcinoma cases (BC070140), 30 cervical carcinoma cases (CR602), 37 rectal cancer cases (RE482), 67 gastric adenocarcinoma cases (BS01012), 40 liver cancer cases (LV483), 40 malignant melanoma cases (ME418a) and 40 prostate cancer cases (PR483a). The TMAs were composed of normal tissue, adjacent tissue and different types of tumor tissues.

IHC analysis

NSCLC tissues were fixed in 10% buffered formalin (Beyotime Institute of Biotechnology, Shanghai, China), embedded in paraffin (Beyotime Institute of Biotechnology) and cut into 5-µm sections. TMAs and NSCLC sections were deparaffinized in xylene (Beyotime Institute of Biotechnology), rehydrated in a series of descending ethanol (Beyotime Institute of Biotechnology) concentrations and incubated in 0.03% hydrogen peroxide (Beyotime Institute of Biotechnology), then stored in dark place for 10 min. Antigen retrieval was performed in 10 mM sodium citrate buffer (pH 6.0; Beyotime Institute of Biotechnology) for 10 min at room temperature. The tissue sections and TMAs were then incubated with antibodies at room temperature for 45 min. Commercial antibodies employed were rabbit monoclonal antibodies: Anti-NLRC5 (1:200; ab117624; Abcam, Cambridge, UK), anti-human leukocyte antigen (HLA)-ABC (1:100; ab70328; Abcam). Following incubation, the specimens were washed with Tris-buffered saline with Tween (TBS-T; 0.5% Tween, 0.1 M Tris-base, 0.9% NaCl; pH 7.6; Beyotime Institute of Biotechnology) and incubated with peroxidase-labeled polymer (Beyotime Institute of Biotechnology) at room temperature for 30 min. The samples were then washed with TBS-T buffer and incubated with freshly prepared 3,3′-diaminobenzidine tetrahydrochloride (DAB; Zhongshan Jinqiao Biological Technology Ltd., Beijing, China) and substrate-chromogen buffer (Beyotime Institute of Biotechnology) at room temperature for 7 min. Immunohistochemical reactions were developed in freshly prepared DAB at room temperature for 7 min, then lightly counterstained with hematoxylin (Beyotime Institute of Biotechnology) prior to mounting. The intensity of staining and the percentage of positive cells were assessed in a semi-quantitative manner. Images were captured using an Olympus BX51 fluorescence microscope (Olympus Corp., Tokyo, Japan) equipped with an Olympus Micro DP 72 camera (Olympus Corp.). The distribution of positive cells was scored as follows: Not stained, 0; <1/3 cells stained, 1; <2/3 cells stained, 2; and >2/3 cells stained, 3. The intensity of staining was graded as follows: Not stained, 0; mild stained, 1; and strong stained, 2. The scores for distribution and intensity were added and graded as follows: 0–2, negative; and 3–5, positive (20).

Statistical analysis

Statistical analysis of the study data was performed using SPSS 17.0 for Windows (SPSS Inc., Chicago, IL, USA). The significance of associations was determined using the Pearson χ2 test. For OS analysis, Kaplan-Meier curves were derived and the statistical significance of differences between the survival of groups with different MHC class I and NLRC5 expression was determined using the log-rank test. The results were censored if the patients remained alive, had died from any other causes or had withdrawn from the study. Cox regression analysis was used for multivariate analysis to allow for comparison of the effects of several different factors on survival. P<0.05 was considered to indicate a statistically significant difference between values.

Results

Correlation of NLRC5 and MHC class I expression in NSCLC patients

NLRC5 and MHC class I expression were detected in 62 cases, including 31 with adenocarcinoma cell cancer, 24 with squamous cell cancer and 7 with other pathology types. IHC staining and analysis revealed that 83.9% of tissues exhibited MHC class I-positive expression, 67.7% of tissues demonstrated cytoplasmic NLRC5-positive expression and 88.7% were nuclear NLRC5-positive (Table I). The association study revealed that the expression of MHC class I was significantly correlated with the expression of nuclear NLRC5 (P=0.008); in addition, nuclear NLRC5 was found to be associated with the expression of NLRC5 in the cytoplasm (P=0.002). However, no correlation was observed between MHC class I and cytoplasmic NLRC5 (P=0.570) (Table II). Fig. 1 shows representative IHC images of HLA-ABC, cytoplasmic and nuclear NLRC5 staining in NSCLC tissues, including negative cytoplasmic and nuclear NLRC5 staining, positive expression of NLRC5 in the cytoplasm and nucleus, HLA-ABC lose and HLA-ABC expression in the tumor cell membrane.

Table I.

MHC class I and NLRC5 expression and association with OS in non-small-cell lung cancer.

Table I.

MHC class I and NLRC5 expression and association with OS in non-small-cell lung cancer.

MarkerExpressionn (%)Median OS (months)95% CIP
MHC class INegative10(16.1)28.019.5–36.50.032
Positive52(83.9)19.016.0–20.0
CNLRC5Negative 7(11.3)32.0 0.0–75.00.086
Positive55 (88.7)19.416.7–22.2
NNLRC5Negative20(32.3)30.024.5–35.50.039
Positive42(67.7)17.014.0–20.0

[i] OS, overall survival; CI, confidence interval; MHC, major histocompatability complex; C/NNLRC5, cytoplasmic/nuclear nucleotide-binding oligomerization-like receptor family caspase recruitment domain-containing 5.

Table II.

Correlation of major histocompatibility complex class I and NLRC5 in seven common human solid tumors.

Table II.

Correlation of major histocompatibility complex class I and NLRC5 in seven common human solid tumors.

HLA-ABC & NNLRC5NNLRC5 & CNLRC5HLA-ABC & CNLRC5
Tumor typenP-valueP-valueP-value
Renal carcinoma 69 0.9260.942 0.703
Gastric adenocarcinoma 67 0.0140.010 0.045
Cervical carcinoma 30 0.2950.363 0.885
Prostate cancer 39 0.0180.746 0.342
Malignant melanoma 40 0.0150.057 0.031
Liver cancer 40 0.0080.002 0.570
Rectal cancer 37 0.0190.812 0.354
All tumor cases384<0.0010.003<0.001

[i] (C/N)NLRC5, (cytoplasmic/nuclear) nucleotide-binding oligomerization-like receptor family caspase recruitment domain-containing 5; HLA-ABC, human leukocyte antigen-ABC.

MHC class I and nuclear NLRC5 indicate the prognosis of NSCLC patients

Nuclear NLRC5 and MHC class I positive expression were revealed to be correlated with a reduced OS rate in NSCLC stage III patients (log-rank, P=0.039 and P=0.032, respectively) (Table I). The median OS of MHC class I-positive patients was 19 months, while the OS for MHC class I-negative patients was 28 months (P=0.032). The median OS of nuclear NLRC5-positive patients was 17 months, while the negative group was 30 months (P=0.039) (Fig. 2). For the cytoplasmic NLRC5-positive and -negative patients, the data were 32 months and 19.4 months, respectively; these results were not significantly associated with prognosis (P=0.086). By contrast, there was no significant association between the expression of MHC class I or NLRC5 and progression free survival (data not shown). Cox regression analysis was used for multivariate analysis to compare the effects of several different factors on survival, including gender, age, pathological type and tumor-node-metastasis values; however, no significant positive correlations were identified (Table III).

Table III.

Association between MHC class I, NLRC5 expressions and clinicopathologic factors in non-small-cell lung cancer patients.

Table III.

Association between MHC class I, NLRC5 expressions and clinicopathologic factors in non-small-cell lung cancer patients.

CharacteristicnHLA-ABC+ (%)PNNLRC5+ (%)PCNLRC5+ (%)P
Gender 0.681 0.349 0.651
Male4841(85.4) 34(70.8) 43(89.6)
Female1411(78.6)  8(57.1) 12(85.7)
Age 0.493 1.00 0.432
>603329(87.9) 22(66.7) 28(84.8)
<602923(79.3) 20(69.0) 27(93.1)
Histological
AC3124(77.4) 21(67.7) 26(83.9)
Classification 0.359 0.401
SC2422(91.7) 16(66.7) 22(91.7)
Others 7 6(85.7)  5(71.4)  7(100.0)
TNM 0.228 0.625 0.406
T1N2M0 3 2(66.7)  1(33.3)  2(66.7)
T2N2M02523(92.0) 17(68.0) 23(92.0)
T3N2M01715(88.2) 12(70.6) 14(82.4)
T4N2M01712(70.6) 12(70.6) 16(94.1)

[i] MHC, major histocompatability complex; (C/N)NLRC5, (cytoplasmic/nuclear) nucleotide-binding oligomerization-like receptor family caspase recruitment domain-containing 5; HLA-ABC, human leukocyte antigen-ABC; AC, adenocarcinoma; SC, squamous carcinoma; TNM, tumor-node-metastasis.

NLRC5 and MHC class I are expressed in different tumor tissues

The expression of NLRC5 and MHC class I were examined in 323 cases of tumor tissue in TMAs by IHC; the tumors investigated were the seven most common types of human solid tumors. The results demonstrated that MHC class I was widely expressed in all seven types of tumor tissue examined and certain sections of the tissues demonstrated high levels of MHC class I expression. The percentages of MHC class I-positive TMAs were 82.6% (57/69) in renal carcinoma, 83.6% (56/67) in gastric adenocarcinoma, 60% (18/30) in cervical squamous carcinoma tissue, 60% (24/40) in prostate cancer, 82.5% (33/40) in malignant melanoma, 67.5% (27/40) in liver cancer and 59.5% (22/37) in rectal cancer. For nuclear and cytoplasmic expression of NLRC5, there results were: 73.9% (51/69) and 88.4% (61/69) in renal carcinoma; 86.6% (58/67) and 77.6% (52/67) in gastric adenocarcinoma; 56.7% (17/30) and 63.3% (19/30) in cervical squamous carcinoma; 85.0% (34/40) and 87.5% (35/40) in prostate cancer; 67.5% (27/40) and 75.0% (30/40) in malignant melanoma; 60% (24/40) and 75.0% (30/40) in liver cancer; and 83.8% (31/37) and 86.5% (32/37) in rectal cancer, respectively (Table IV). Fig. 3 shows the immunohistochemical staining of seven human solid tumor tissue microarrays. Each panel shows a representative example of tumor tissue exhibiting positive HLA-ABC, cytoplasmic NLRC5 and nuclear NLRC5 staining.

Table IV.

Expression of major histocompatibility complex class I and NLRC5 in seven common human solid tumors.

Table IV.

Expression of major histocompatibility complex class I and NLRC5 in seven common human solid tumors.

Tumor typenHLA-ABC+ (%)CNLRC5+ (%)NNLRC5+ (%)
Renal carcinoma6957 (87.6)61 (88.4)51 (73.9)
Gastric adenocarcinoma6756 (83.6)52 (77.6)58 (86.6)
Cervical carcinoma3018 (60.0)19 (63.3)17 (56.7)
Prostate cancer4024 (60.0)35 (87.5)34 (85.0)
Malignant melanoma4033 (82.5)30 (75.0)27 (67.5)
Liver cancer4027 (67.5)30 (75.0)24 (60.0)
Rectal cancer3722 (59.5)32 (86.5)32 (83.8)

[i] (C/N)NLRC5, (cytoplasmic/nuclear) nucleotide-binding oligomerization-like receptor family caspase recruitment domain-containing 5; HLA-ABC, human leukocyte antigen-ABC.

Correlation of NLRC5 and MHC class I expression in tumors

In the 385 cases (62 NSCLC and 323 TMAs) of tumor paraffin-tissues for IHC analysis, the expression of MHC class I (HLA-ABC), cytoplasmic NLRC5 and nuclear NLRC5 were examined and their correlations were determined using the Pearson χ2 test. The results revealed significant correlations between MHC class I and nuclear NLRC5 (P<0.001), MHC class I and cytoplasmic NLRC5 (P=0.003) and between nuclear and cytoplasmic NLRC5 (P<0.001) (Table II). Furthermore, the correlations between the three proteins expression were analyzed in the seven TMAs separately. The results revealed that, with the exception of renal carcinoma and cervical cancer, all the tumor tissues demonstrated correlations between MHC class I and nuclear NLRC5 expression (Table II). These results indicated that, as a MHC class I transactivitor, the expression of NLRC5 was correlated with MHC class I in human solid tumors.

Discussion

To the best of our knowledge, the present study was the first to examine the expression of NLRC5 in common human tumor tissues and its association with the clinical outcomes of NSCLC stage III patients. The results revealed that NLRC5 and MHC class I expression were detected in NSCLC and seven other types of common human tumor tissues. IHC staining demonstrated that NLRC5 was expressed in the nucleus and cytoplasm of all eight common tumor tissues. In addition, the expression of MHC class I was found to be associated with nuclear NLRC5 in all 385 tumor cases. These results indicated that as in normal immune situations, NLRC5 regulates MHC class I expression in human tumors. By analyzing the clinical data of 62 postoperative NSCLC stage III patients, it was determined that MHC class I and nuclear NLRC5 expression were independent predictors of poor survival, which was consistent with certain previous studies (7,21,22).

In the present study, there was a high level of consistency among the 62 NSCLC patients, as they all underwent radical surgery and were diagnosed with stage III-N2 NSCLC. This may reduce the effects of difference between various tumor stages and increase credibility of the current results. In the present study, the individual IHC results for the NSCLC, liver cancer, gastric adenocarcinoma, rectal cancer, malignant melanoma tissues all revealed a correlation between the expression of MHC class I and nuclear NLRC5. However, in the renal and cervical carcinoma cases, there was no significant correlation between MHC class I and NLRC5 (cytoplasmic and nuclear) expression. This may be due to the limited number of cases for cervical cancer. While in renal carcinoma, the majority of the tumor is clear cell carcinoma, which is adenocarcinoma of the renal tubular epithelial cell; therefore, the tissue heterogeneity was different from the other tumor types examined.

Due to the role of MHC class I molecules in tumor immune surveillance and immune evasion, a number of studies have aimed to elucidate the mechanisms by which this proceeds and its association with patient prognosis (2,23). Previous studies have suggested that high levels of MHC class I expression makes tumor cells promising targets for T cells; by contrast, weak expression prevents specific T cell recognition and results in an increased risk of disease recurrence (3,24). For colorectal cancer, Simpson et al (5) reported a mean survival advantage of 26.1 months in patients whose tumors had strong MHC class I expression over those who exhibited weak MHC class I expression. Nagata et al demonstrated that HLA class I loss was associated with recurrence-free survival time, but not OS in NSCLC (25). However, certain studies reached different conclusions. Madjd et al (7) reported that the total loss of MHC class I was an independent indicator of positive prognosis in breast cancer. In addition, Ramnath et al (8) suggested that HLA class I antigen downregulation was associated with improved survival (8). In certain other types of tumors, the results also varied (2630). MHC class I loss may affect antigen presentation to T-lymphocytes and CTL function; however, this may increase the susceptibility of tumors to NK cells and result in an improved prognostic outcome. Ramnath et al (8) indicated that there was a selective loss of MHC class I heavy chain, which was associated with improved prognosis. This may be the result of immune surveillance, which in certain patients may select against the more aggressive tumors, allowing for the growth of the more indolent HLA-negative tumors. Tumor growth may then be further controlled by NK cells (8). These previous results demonstrated that in different tumor types, T cell recognition and NK cell function were not identical and may therefore have various effects on tumor growth and patient survival.

The results of previous studies regarding MHC class I as a prognostic indicator have been controversial; this may be due to the types of samples included these studies. Certain studies have analyzed tumor patients at different disease stages with short clinical follow up (7,8,25). Analysis of various tumor stages in a small group of patients may not be sufficient to determine whether MHC class I may be used as a prognostic indicator. The present study included 62 highly consistent cases of NSCLC stage III patients; therefore, these results may be more representative and indicate a novel method for predicting the prognosis of NSCLC patients. Further studies are required, with large-sample randomized experiments in order to confirm the potential of MHC class I and nuclear NLRC5 as prognostic factors for different types of cancer.

The function of NLRC5 as a MHC class I transactivator has been studied thoroughly over the past few decades. NLRC5 moves between the cytoplasm and nucleus, which indicates that it may have a nuclear function (31). The expression of NLRC5-mediated MHC class I gene requires an intact nuclear localization signal and nuclear distribution (31). Therefore, altered cellular localization of NLRC5 may impact MHC class I expression as well as MHC class I-mediated antigen presentation (9). In addition, it was reported that NLRC5 influences histone methylation (H3K27me3) and may therefore mediate gene expression through adjusting the chromosome activation status of the MHC class I locus (32). In the present study, nuclear and cytoplasmic NLRC5 expression were found to be associated with MHC class I (P<0.001 and P=0.003, respectively).

In conclusion, the results of the present study demonstrated that NLRC5 was widely expressed in eight common human tumor tissues in the nucleus as well as the cytoplasm. Furthermore, the nuclear expression was found to be correlated with MHC class I. MHC class I heavy chain loss has been validated in a previous study to be a predictor of patient survival (22); the present study demonstrated that the expression of NLRC5 in the nucleus acted as a negative prognostic indicator in NSCLC patients. Therefore NLRC5 and MHC class I may be used in conjunction with other independent prognostic factors in order to further stratify patients for adjuvant therapy. However, in order to validate the use of these factors as cancer biomarkers to predict the patients' prognosis, randomized screening trials are required. In vitro and in vivo experiments may also be required in order to fully elucidate the effect of MHC class I and NLRC5 on the tumor growth and differentiation.

Acknowledgements

The authors would like to thank Miss. Li Li for advice and instruction in IHC and Professor Chen Xian-Cheng for assistance with microscopy and image processing.

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September-2015
Volume 10 Issue 3

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Copy and paste a formatted citation
x
Spandidos Publications style
Li X, Guo F, Liu Y, Chen HJ, Wen F, Zou B, Li D, Qin Q, Liu X, Shen Y, Shen Y, et al: NLRC5 expression in tumors and its role as a negative prognostic indicator in stage III non-small-cell lung cancer patients. Oncol Lett 10: 1533-1540, 2015.
APA
Li, X., Guo, F., Liu, Y., Chen, H., Wen, F., Zou, B. ... Wang, Y. (2015). NLRC5 expression in tumors and its role as a negative prognostic indicator in stage III non-small-cell lung cancer patients. Oncology Letters, 10, 1533-1540. https://doi.org/10.3892/ol.2015.3471
MLA
Li, X., Guo, F., Liu, Y., Chen, H., Wen, F., Zou, B., Li, D., Qin, Q., Liu, X., Shen, Y., Wang, Y."NLRC5 expression in tumors and its role as a negative prognostic indicator in stage III non-small-cell lung cancer patients". Oncology Letters 10.3 (2015): 1533-1540.
Chicago
Li, X., Guo, F., Liu, Y., Chen, H., Wen, F., Zou, B., Li, D., Qin, Q., Liu, X., Shen, Y., Wang, Y."NLRC5 expression in tumors and its role as a negative prognostic indicator in stage III non-small-cell lung cancer patients". Oncology Letters 10, no. 3 (2015): 1533-1540. https://doi.org/10.3892/ol.2015.3471