Skip to main content

HIF-1α and Caspase-3 expression in aggressive papillary thyroid carcinoma



Tumor cells adapt to hypoxia by regulating transcription factors that involved in regulation of metabolism, angiogenesis, cell proliferation, and apoptosis. Under hypoxic conditions, hypoxia-inducible factor-1 (HIF-1), consisting of HIF-1α and HIF-1β subunits, acts as a key transcription factor mediating the adaptive cellular responses. Caspase-3 is a key apoptosis-related protease that plays a role in tumor growth and development. Studies have shown that caspase-3 could be regulated by HIF-1α under pathological conditions. Therefore, HIF-1α and caspase-3 expression may be related to the poor prognosis of tumors. In this study, we analyzed the possible relationships between these two signaling factors in correlation with the clinical behavior of PTC.


We detected the expression levels of HIF-1α and caspase-3 in 70 samples of PTC and para-cancerous tissues (control group) by immunohistochemistry (IHC). Furthermore, various clinicopathological parameters were assessed to determine their correlations with HIF-1α and caspase-3 expressions.


First, HIF-1α and caspase-3 expressions (60% and 37.1%, respectively) increased significantly in the PTC samples as compared to normal tissues (2.9% for both HIF-1α and caspase-3) (p < 0.05) as determined by IHC. Second, although there was no significant difference between the expression of HIF-1α and caspase-3 in regard to gender, age distribution, tumor size, lymph node metastasis, and BRAFV600E mutation (all p > 0.05), HIF-1α and caspase-3 expressions were associated with capsule invasion and cell subtypes of PTC (p < 0.05). The percent positivity of caspase-3 expression in tall-cell variant (TCV) was the highest (63.6%). Third, HIF-1α expression was positively correlated with that of caspase-3 (rs = 0.326; p < 0.05).


Overexpression of HIF-1α and caspase-3 is associated with carcinogenesis. These factors might serve as promising predictors of aggressive PTC. These findings also suggest their potential as therapeutic targets.


Thyroid cancer is one of the most commonly seen endocrine malignancies, with an increasing annual incidence rate worldwide [1]. The majority of thyroid cancers originate from follicular epithelial cells. Of these subtypes, papillary thyroid carcinoma (PTC) accounts for about 85% of the overall cases. Although PTC carries a 5-year survival rate of 97%, about 15% of patients who relapse present with clinical symptoms of aggressive PTC, such as local tissue infiltration, cervical lymph node metastasis (CLNM), and even distant metastasis at an early stage [2,3,4]. Therefore, it is crucial to diagnose and treat aggressive PTC at the early stage of symptomatic manifestations.

The tumor microenvironment (TME) plays a significant role in the growth and metastasis of most cancers. Hypoxic condition within the TME has been found to be crucial in different stages of tumor development. Under hypoxic conditions, tumor cells adapt to hypoxia by transcription factors that involved in regulation of metabolism, angiogenesis, cell proliferation, and apoptosis. Hypoxia-inducible factor-1 (HIF-1), consisting of HIF-1α and HIF-1β subunits, is a key transcription factor that mediates these adaptive cellular responses [5]. Liu et al. have found that the decrease in cellular oxygen level is related to the poor prognosis of PTC patients [6]. Therefore, the induction of HIF-1α expression can promote the aggressiveness of tumors.

However, the underlying molecular mechanisms are not fully understood. Some studies have reported that the transcription of several apoptosis-related genes, including survivin, Bcl-2, and caspase-3, could be regulated by HIF-1α [7, 8]. Caspase-3 is shown to act as a key protease during apoptosis as well as in tumor growth and development. To date, none of the studies has systematically assessed the expression profiles of both HIF-1α and caspase-3 and their associated signaling pathways in PTC.

Therefore, we aimed to analyze the expressions of HIF-1α and caspase-3 to reveal the possible cross talk between these two factors and explore their correlations with the patho-clinical behaviors of PTC.


Patients and specimens

This study recruited 80 PTC patients who received thyroidectomy at our hospital, between January 2019 and June 2019. We excluded 10 patients with Hashimoto thyroiditis. Biopsies of the remaining 70 PTC patients were subjected to immunohistochemistry (IHC) to assess HIF-1α and caspase-3 expressions, and the relatively normal para-cancerous tissues were used as controls. The carcinoma samples were additionally analyzed to detect the BRAFV600E mutation.

The inclusion criteria were as follows: (1) patients did not receive any treatments prior to thyroidectomy; (2) ultrasound data was complete; (3) PTC diagnosis, capsule invasion, and CLNM were pathologically confirmed; (4) the absence of any other carcinomas was confirmed; (5) sufficient amount of DNA were extracted from biopsy samples to detect the BRAFV600E mutation; and (6) patients who had total thyroidectomy underwent the central neck dissection.

This study was approved by the ethics committee of our hospital. As this is a retrospective study, informed consent was waived.

Cell subtype determination

All formalin-fixed paraffin-embedded (FFPE) tumor tissues were sliced into 4 μm sections, and one slide for each tissue sample was subjected to the hematoxylin and eosin staining. All histological slides were reviewed by pathologists to identify cell subtypes of PTC, including tall-cell variant (TCV), classic variant of papillary thyroid carcinoma (CVPTC), and follicular variant of papillary thyroid carcinoma (FVPTC), by a light microscope. The tumor area was marked to extract genomic DNA.

Analysis of the BRAFV600E mutation

Genomic DNA was extracted from paraffin-embedded tissues of PTC patients. Under the manufacturer’s instructions, the process was performed using an FFPE DNA Kit (Cat No. ADx-FF01, Xiamen, China). The A260:A280 values ranged from 1.7 to 1.9. The DNA samples were then subjected to the next-generation sequencing (NGS) to determine BRAFV600E genotypes (Beijing Jingkerui Biotechnology Co., Ltd., Beijing, China).

Immunohistochemistry staining

Paraffin-embedded blocks were sectioned to 4 μm thickness. After de-paraffinization and rehydration, antigen retrieval was carried out by boiling the tissue slide in EGTA antigen retrieval solution (Zhongshan Golden Bridge Biotechnology, China, pH 8.0) and then washing the section with phosphate-buffered saline (PBS). Thyroid sections were incubated with rabbit antihuman HIF-1α (1:200, Zhongshan Golden Bridge Biotechnology, China) and rabbit anti-human caspase-3 (1:500, Cell Signaling Technology, Danvers, MA, USA) at 4 °C overnight. After three washes with PBS, secondary antibodies (Maixin Biotechnology Co., Ltd.) were added to the sections, followed by counterstaining with hematoxylin and observation with a microscope. All slides were reviewed and evaluated by three pathologists who were blinded to the clinical data.

Stromal staining of HIF-1α and caspase-3 expressions was graded using a quick score (QS) system. The QS represents the sum of a proportional score (PS) and intensity score (IS). The PS was classified into five levels: 0: 0–5%; 1: 6–25%; 2: 26 to 50%; 3: 51–75%; 4: 76 to 100%, while the IS was graded as follows: −(0), +(1), ++(2), and +++(3). The QS was defined as follows: 0–3 scores were regarded as negative and 4–7 scores as positive [9].

Statistical analysis

Statistical analyses were performed using the SPSS version 16.0 (SPSS, Inc., Chicago, USA). Pearson’s chi-square test was used for categorical variables. The correlation between HIF-1α and caspase-3 expressions was evaluated by Spearman correlation analysis. A p-value of < 0.05 was considered statistically significant. To identify risk factors for capsule invasion in PTC, a multivariate logistic regression analysis was performed.


Expressions of HIF-1α and caspase-3 in PTC and normal tissues

Both HIF-1α and caspase-3 expressions in 70 PTC samples and their relatively normal para-carcinoma tissues were detected by IHC. The positive staining of HIF-1α and caspase-3 was located in the cytoplasm (Fig. 1). The results showed that HIF-1α and caspase-3 expressions (60% and 37.1%, respectively) increased significantly in the PTC samples as compared to that in normal tissues (both expression levels were 2.9%) (p < 0.05; Fig. 1 and Table 1). This indicated that HIF-1α and caspase-3 were involved in the carcinogenesis of PTC.

Fig. 1
figure 1

Representative images of HIF-1α and caspase-3 expression in papillary thyroid carcinoma (PTC). A Expression of HIF-1α in PTC. B Expression of HIF-1α in normal tissues. C Expression of caspase-3 in PTC. D Expression of caspase-3 in normal tissues. Magnification is ×100

Table 1 HIF-1α and caspase-3 expression in PTC and normal tissues

Correlations of HIF-1α and Caspase-3 expressions with clinicopathological parameters

A total of 70 consecutive patients, including 58 females and 12 males, were used for data analysis. The mean age was 44 ± 12 years. There were no significant differences between HIF-1α and caspase-3 expressions with respect to gender, age distribution, and tumor size (all p > 0.05; Table 2). Additionally, HIF-1α expression was significantly associated with capsule invasion (p < 0.05; Table 2). However, caspase-3 expression indicated no notable correlation with capsule invasion (p > 0.05, Table 2).

Table 2 Clinicopathological features of patients with PTC

Both LNM and BRAFV600E mutation exhibited no significant differences in HIF-1α expression levels (all p > 0.05; Table 2), as well as in caspase-3 levels (all p > 0.05; Table 2).

Furthermore, the level of caspase-3 expression was specific to PTC cell type (p < 0.05; Table 2). The percent positivity of caspase-3 expressions in TCV, CVPTC, and FVPTC was 63.6%, 48%, and 20.6%, respectively.

However, HIF-1α expression showed no significant difference among different PTC cell subtypes (p > 0.05; Table 2).

The correlative relationship between HIF-1α and caspase-3 expression

The correlation between HIF-1α and caspase-3 expression was evaluated by the Spearman correlation analysis as listed in Table 3. The positive expression of HIF-1α was significantly associated with that of caspase-3 (rs = 0.326; p < 0.05; Table 3).

Table 3 Association between HIF-1α and caspase-3 expression

Univariate analysis for capsule invasion in PTC

The univariate analysis of clinicopathological features revealed that tumor size and HIF-1α-positive expression were significantly different between PTCs with and without capsule invasion (p < 0.05; Table 4). However, no significant difference was detected between the two groups in gender, age, BRAFV600E mutation, cell subtypes, and caspase-3 expression (all p > 0.05, Table 4).

Table 4 Predictive factors of capsule invasion in PTC


In most cases, PTC is regarded as an indolent tumor which has a favorable prognosis. However, cell subtype, tumor size, and the expression of carcinoma markers may affect the prognosis, while the underlying molecular pathomechanism remains elusive so far. This study identified that cytoplasmic expression of HIF-1α was present in 60% of PTC patients, compared to para-carcinoma tissues (2.9%), which was consistent with previous reports [10, 11]. This indicated that HIF-1α might play important transcriptional and regulatory roles at an early stage of PTC.

Recent studies have revealed that HIF-1α expression is upregulated in solid tumors such as colorectal carcinoma [12], hepatocellular carcinoma [13], and thyroid cancer [14]. Although PTC has a mortality rate of less than 5%, there is still a small number of patients with metastasis or relapse. HIF-1α, as one of the HIF family members, is critically related to tumor metastasis and tumor staging [15]. In PTC, increased HIF-1α level is associated with CLNM and distant metastasis [6, 16]. Our study assessed relationships between the HIF-1α expression and several clinicopathological parameters in PTC patients. As a result, HIF-1α expression showed no significant differences among PTC patients in terms of gender, age distribution, and tumor size, which were consistent with previous findings [6]. Pathological type and BRAFV600E mutation status were considered important prognostic factors for PTC patients. We analyzed the correlations between cell subtypes, BRAFV600E mutation, and HIF-1α expression and found that there was no significant association of the proportion of cell subtypes with BRAFV600E mutation status.

Like other tumors, thyroid carcinoma has biological characteristics of infiltration and metastasis, even breaking through the capsule into surrounding nerves and muscles. This study showed high levels of HIF-1α expression in PTC patients with capsule invasion. Previous studies have confirmed that capsule invasion is one of the major risk factors for LNM [17, 18]. Thus, this study suggests that HIF-1α expression may be related to LNM pathogenesis. Unfortunately, LNM showed no significant differences with or without HIF-1α expression, which was contradictory to a previous report [6], and that might be due to the small sample size used in our study. Together, these results suggest that HIF-1α induction may be involved in the invasion of PTC. Whether HIF-1α expression correlates with metastasis in PTC needs further investigations. Some clinical features, such as TNM staging and distant metastasis, should be included in the prognosis of PTC patients.

Recent studies indicate that HIF-1α regulates invasion, metastasis, and prognostic evaluation in PTC through various mechanisms [11, 16, 19]. As we know, solid tumors generally possess hypoxic microenvironments during their development. Under hypoxic conditions, HIF-1α could bind to HIF-1β to form the HIF-1 complex that can promote the transcription of downstream genes involved in angiogenesis, tumor invasion, and metastasis by binding to the hypoxia response element (HRE) of the gene promoters to regulate their expressions [20]. Thus, HIF-1α upregulates the expression of these genes to promote invasion and metastasis of PTC.

Caspase-3 has been reported as a key protease in the apoptosis process [21]. Recently, Huang et al. have found that the high level of caspase-3 in patients is associated with head and neck cancers [22]. Thyroid cancer is one of the common head and neck cancers. There are a few research studies on the caspase-3 expression in thyroid cancer. In this study, the expression of caspase-3 was significantly associated with the occurrence of PTC. Notably, the caspase-3 expression did not show any significant differences in gender, age distribution, tumor sizes, and the BRAFV600E mutation status. However, caspase-3 expression was significantly associated with the PTC subtype. It was higher in TCV (63.6%) than in any other cell subtype. About 20.6% of FVPTC patients presented caspase-3-positive expression. This indicated that caspase-3 might be related to aggressive tumor behavior and prognosis and was consistent with previous studies [23, 24]. LNM is considered a significant aggressive tumor behavior. Therefore, we analyzed the caspase-3 expression in PTC patients with LNM. Possibly due to the small sample size, we could not detect any significant difference in caspase-3 expression between LNM and non-LNM groups. Furthermore, HIF-1α expression was positively associated with that of caspase-3 in PTC (rs = 0.326; p < 0.05). However, there were no significant differences in caspase-3 expressions in PTC patients with capsule invasion.

These results suggest that caspase-3 expression may correlate to aggressive behavior in PTC. PTC patients with high caspase-3 expressions may be at higher risks for LNM, distant metastasis, and low survival rates. These parameters should be included to analyze the relationship between caspase-3 and clinical prognosis in future studies. Recently, it has been shown that caspase-3 could promote oncogenic transformation by inducing genetic instability [25]. This might explain why caspase-3 expression was high in TCV. The molecular mechanism remains to be further explored.

Therefore, HIF-1α and caspase-3 might be used as potential biomarkers for the diagnosis as well as therapeutic targets for aggressive PTC cases. Moreover, we found that tumor sizes of ≥ 1.0 cm along with increased HIF-1α expression were independent predictors of the risk of capsule invasion. Further studies are warranted to explore predictors of capsule invasion.

There are several limitations in this study. First, it was a single-institution retrospective observational study, which might have selection bias. Second, the sample size was not statistically large; therefore, we could not arrive at a definitive conclusion about the involvement of LNM and BRAFV600E mutation in PTC aggression and prognosis. A large-scale study will be necessary to determine the exact pathological roles of these molecules in the diagnosis and prognosis of PTC. Third, survival and death of PTC patients were not analyzed in our study; therefore, we could not observe their hard points. We will collect more cases and track their hard points to evaluate their prognostic value in our post-study.


Overexpression of HIF-1α and caspase-3 could be associated with PTC. For the first time, we reported the positive correlation between HIF-1α and caspase-3 expression in PTC. They are promising predictors of aggressive PTC and may serve as new therapeutic targets for PTC treatment.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.



Hypoxia-induced factor 1α


Papillary thyroid carcinoma




Tumor microenvironment


Cervical lymph node metastasis


Formalin-fixed paraffin-embedded


Classic variant of papillary thyroid carcinoma


Follicular variant of papillary thyroid carcinoma


Tall-cell variant


Next-generation sequencing


Phosphate-buffered saline


Quick score


Proportional score


Hypoxia response element


  1. Davies L, Welch HG. Current thyroid cancer trends in the United States. JAMA Otolaryngol Head Neck Surg. 2014;140:317–22.

    Article  PubMed  Google Scholar 

  2. Orosco RK, Hussain T, Brumund KT, Oh DK, Chang DC, Bouvet M. Analysis of age and disease status as predictors of thyroid cancer-specific mortality using the Surveillance, Epidemiology, and End Results database. Thyroid. 2015;25:125–32.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Wang N, Duan H, Zhang C, Zhou Y, Gao R. The LINC01186 suppresses cell proliferation and invasion ability in papillary thyroid carcinoma. Oncol Lett. 2018;16:5639–44.

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Siegel RL, Miller KD, Jemal A. Cancer Statistics, 2017. CA Cancer J Clin. 2017;67:7–30.

    Article  PubMed  Google Scholar 

  5. Sethi K, Rao K, Bolton D, Patel O, Ischia J. Targeting HIF-1alpha to prevent renal ischemia-reperfusion injury: does it work? Int J Cell Biol. 2018;2018:9852791.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Liu YM, Ying SP, Huang YR, Pan Y, Chen WJ, Ni LQ, et al. Expression of HIF-1alpha and HIF-2alpha correlates to biological and clinical significance in papillary thyroid carcinoma. World J Surg Oncol. 2016;14:30.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Delbrel E, Soumare A, Naguez A, Label R, Bernard O, Bruhat A, et al. HIF-1alpha triggers ER stress and CHOP-mediated apoptosis in alveolar epithelial cells, a key event in pulmonary fibrosis. Sci Rep. 2018;8:17939.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Zhao Q, Tan BB, Li Y, Fan LQ, Yang PG, Tian Y. Enhancement of drug sensitivity by knockdown of HIF-1alpha in gastric carcinoma cells. Oncol Res. 2016;23:129–36.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Zeming L, Wen Z, Yusufu M, Jie M, Yawen G, Yan L, et al. High expression of yes-activated protein-1 in papillary thyroid carcinoma correlates with poor prognosis. Appl Immunohistochem Mol Morphol. 2019;27:59–64.

    Article  Google Scholar 

  10. Koperek O, Akin E, Asari R, Niederle B, Neuhold N. Expression of hypoxia-inducible factor 1 alpha in papillary thyroid carcinoma is associated with desmoplastic stromal reaction and lymph node metastasis. Virchows Arch. 2013;463:795–802.

    Article  CAS  PubMed  Google Scholar 

  11. Semenza GL. Hypoxia-inducible factors: mediators of cancer progression and targets for cancer therapy. Trends Pharmacol Sci. 2012;33:207–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Maria IEP, Korina B. 2015-HIF-1α in colorectal carcinoma review of the literature. J BUON. 2015;20:680–9.

    Google Scholar 

  13. Yang SL, Liu LP, Jiang JX, Xiong ZF, He QJ, Wu C. The correlation of expression levels of HIF-1alpha and HIF-2alpha in hepatocellular carcinoma with capsular invasion, portal vein tumor thrombi and patients' clinical outcome. Jpn J Clin Oncol. 2014;44:159–67.

    Article  PubMed  Google Scholar 

  14. Jozwiak P, Ciesielski P, Zaczek A, Lipinska A, Pomorski L, Wieczorek M, et al. Expression of hypoxia inducible factor 1alpha and 2alpha and its association with vitamin C level in thyroid lesions. J Biomed Sci. 2017;24:83.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Zhang J, Wu Y, Lin YH, Guo S, Ning PF, Zheng ZC, et al. Prognostic value of hypoxia-inducible factor-1 alpha and prolyl 4-hydroxylase beta polypeptide overexpression in gastric cancer. World J Gastroenterol. 2018;24:2381–91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Klaus A, Fathi O, Tatjana T-W, Bruno N, Oskar K. Expression of hypoxia-associated protein HIF-1α in follicular thyroid cancer is associated with distant metastasis. Pathol Oncol Res. 2017;24:289–96.

    Article  PubMed  Google Scholar 

  17. Xu SY, Yao JJ, Zhou W, Chen L, Zhan WW. Clinical characteristics and ultrasonographic features for predicting central lymph node metastasis in clinically node-negative papillary thyroid carcinoma without capsule invasion. Head Neck. 2019;41:3984–91.

    Article  PubMed  Google Scholar 

  18. Kamaya A, Tahvildari AM, Patel BN, Willmann JK, Jeffrey RB, Desser TS. Sonographic detection of extracapsular extension in papillary thyroid cancer. J Ultrasound Med. 2015;34:2225–30.

    Article  PubMed  Google Scholar 

  19. Zhou L, Cha G, Chen L, Yang C, Xu D, Ge M. HIF1alpha/PD-L1 axis mediates hypoxia-induced cell apoptosis and tumor progression in follicular thyroid carcinoma. OncoTargets Ther. 2019;12:6461–70.

    Article  CAS  Google Scholar 

  20. Zhao T, Jin F, Xiao D, Wang H, Huang C, Wang X, et al. IL-37/ STAT3/ HIF-1alpha negative feedback signaling drives gemcitabine resistance in pancreatic cancer. Theranostics. 2020;10:4088–100.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Heidari Z, Eskandari M, Aryan A, Rostamzad F, Salimi S. The effect of CASP3 rs4647610 and rs4647602 polymorphisms on tumour size and cancer stage in papillary thyroid carcinoma. Br J Biomed Sci. 2020;77:129–34.

    Article  CAS  PubMed  Google Scholar 

  22. Huang Q, Li F, Liu X, Li W, Shi W, Liu FF, et al. Caspase 3-mediated stimulation of tumor cell repopulation during cancer radiotherapy. Nat Med. 2011;17:860–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Mishunina TM, Kalinichenko OV, Tronko MD, Statsenko OA. Caspase-3 activity in papillary thyroid carcinomas. Exp Oncol. 2010;32:269–72.

    CAS  PubMed  Google Scholar 

  24. Lamba Saini M, Bouzin C, Weynand B, Marbaix E. An appraisal of proliferation and apoptotic markers in papillary thyroid carcinoma: an automated analysis. PLoS One. 2016;11:e0148656.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Liu X, He Y, Li F, Huang Q, Kato TA, Hall RP, et al. Caspase-3 promotes genetic instability and carcinogenesis. Mol Cell. 2015;58:284–96.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references


Thanks to my colleagues for help.


This study was supported in part by grants from the Research Foundation of Beijing Friendship Hospital, Capital Medical University (No. yyqdkt2019-18).

Author information

Authors and Affiliations



LQ and LZ designed the research. BS and YH conducted the experiment. LZ analyzed the data and wrote the paper. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Linxue Qian.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Ethics Committee of the Beijing Friendship Hospital affiliated to Capital Medical University. As this is a retrospective study, informed consent was waived.

Consent for publication

No applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhang, L., Shi, B., Hu, M. et al. HIF-1α and Caspase-3 expression in aggressive papillary thyroid carcinoma. World J Surg Onc 20, 353 (2022).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • HIF-1α
  • Caspase-3
  • Thyroid carcinoma